ESPE Abstracts

Contents

• Plenary Lectures
• • RANKL and RANK: Bone and Beyond
  • • RANKL and RANK: Bone and Beyond

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  • Light, Body Clocks and Sleep: Biology to New Therapeutics
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  • Glucocorticoid Rhythms, Stress Response and the Brain from Neonates to Adults
  • • Glucocorticoid Rhythms, Stress Response and the Brain from Neonates to Adults

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  • Development of Novel Therapies for Obesity
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  • HPG -Nutrition and the Hypothalamo-Pituitary-Gonadal Axis
  • • Nutrition and the Reproductive Axis: Implications for the Control of Puberty

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  • How to Reduce Waste and Increase Value in Translational Biomedical Research
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  • Pituitary Gigantism - An Update
  • • Pituitary Gigantism – an Update

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  • Novel Advances in Artificial Pancreas Development
  • • Novel Advances in Artificial Pancreas Development

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• Symposia
• • Novel Advances in Diabetes and Obesity
  • • Off the Weight Curve – Dynamics of Childhood Obesity

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    • The Gut Microbiome and Obesity

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    • Rare Genetic Forms of Obesity: Clinical Approaches and Current Treatments in 2019

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  • Novel Mechanisms and Therapies in Bone and Growth Plate: Investing in the Future Health of Children
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    • Anabolic Therapies for Osteoporosis in Childhood

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    • Glucocorticoid-Induced Osteoporosis in Children: Targeting the Spine in Osteoporosis Diagnosis, Monitoring and Treatment

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  • Novel Insights in Our Understanding of Disorders of Sex Development: From Genes to Clinical Outcomes
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    • Abstract unavailable

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    • Novel Insights into Sex Determination: Mutual Antagonism of Pro-Testis and Pro-Ovary Signalling Pathways

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  • ISPAD/Complications of Type 1 Diabetes
  • • Hypoglycemia in Children with T1D: Past, Present, and Future

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    • Novel Advances in Diabetic Retinopathy Screening and Management

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    • Prediction of Renal and Cardiovascular Complications

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  • Impact of Genomics on Growth
  • • Novel Insights into Genetic Disorders of Growth

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    • SHOX: From Basic Research to Complex Models and Therapy

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    • The Role of KCNQ1 in Pituitary Development

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  • Endocrinology Meets Diversity: Transgender Youth
  • • Impact of Cross-Sex Hormone Treatment on Structural Brain Networks

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    • Psychiatric Comorbidities in Transgender Youth

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    • Gynecological Aspects and Fertility Issues in Transgender Adolescents

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  • Adrenal Insufficiency: New Mechanisms, New Therapies
  • • Novel Interventions to Treat Adrenal Insufficiency

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    • Novel Insights into the Pathophysiology of Adrenal Insufficiency Syndromes

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    • Widening the Horizon - Clinical Relevance of Steroid Hormone Pathways

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  • Autoimmunity: From Diagnosis to Treatment
  • • New Autoantibodies in Endocrine Autoimmunity Development: Lessons from APECED

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    • Monogenic Forms of Autoimmune Diabetes: Challenges and Opportunities

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    • Abstract unavailable

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  • Heterogeneity of Paediatric Diabetes
  • • Diversity in Monogenic Diabetes Management and Prognosis

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    • Diagnostic and Therapeutic Implications of Double Diabetes

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    • Obesity Distorting Childhood Diabetes: Is it Type 2, Type 1, or MODY? A Pathophysiological Perspective

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  • Brain development and sex: Is it Chromosomes or Hormones?
  • • Multifaceted Origins of Sex Differences in the Brain

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    • Abstract unavailable

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    • How Hormones Impact on Emotion and Cognition – New Insights From Magnetic Resonance Imaging

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  • Recent Advances in our Understanding of Hypogonadotrophic Hypogonadism
  • • Novel Insights into Developmental Pleiotropy From Genetic Studies in Kallmann Syndrome

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    • Novel Insights into the Regulation of Reproduction Using 3D-Imaging in Transparent Fetuses and Postnatal Animals

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    • Abstract unavailable

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• Special Symposia
• • (1)
  • • E-Learning in Paediatric Endocrinology and Diabetes in Resource Limited Countries (RLC)

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    • E-learning ESPE interactive case

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• Meet the Expert
• • Holistic Approach to the Individual with DSD
  • • Holistic Approach to the Individual with DSD

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  • The Use of MRI as a Diagnostic Tool in Neuroendocrine Disorders
  • • The Interpretation of Abnormal Thyroid Function in Tests in Children and Adolescents

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  • Turner syndrome - Clinical Practice Guidelines for the Care of Girls and Women with Turner Syndrome: Proceedings from the 2016 Cincinnati International - Turner Syndrome Meeting
  • • New International Guidelines on Turner Syndrome

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  • Klinefelter Syndrome - when should Testosterone be Started
  • • Klinefelter Syndrome - When Should Testosterone be Started?

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  • Managing Endocrinopathies in McCune-Albright Syndrome
  • • Managing Endocrinopathies in McCune-Albright Syndrome

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  • Insulin Dosing for Real Meals
  • • Insulin Dosing for Real Meals

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  • Management of Graves Disease
  • • Management of Graves' Disease

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  • Management of Neonatal Hypoglycaemia
  • • Management of Neonatal Hypoglycaemia

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• How Do I
• • How Do I Session 1
  • • Management of Subclinical Hypothyroidism

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    • Abstract unavailable

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    • Management of Insulin Resistance in Children

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  • How Do I Session 2
  • • How do I…. Manage Micropenis in a Child

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    • How Do I Diagnose Growth Hormone Insensitivity

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    • Management of an Asymptomatic Child with T1D and Transglutaminase Positivity

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• Novel Advances
• • Stem Cell Reprogramming, IPS Cells
  • • Abstract unavailable

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  • Genomic Imprinting Analysis in Clinical Practice
  • • Genomic Imprinting Analysis in Clinical Practice

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• Controversies
• • Does Obesity Need Tertiary Care Provision?
  • • Abstract unavailable

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    • Does Obesity Need Tertiary Care Provision? – Against !

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• Young Investigators
• • (1)
  • • Abstract unavailable

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    • Early Life Events and Postnatal Effects from Infancy to Childhood

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• Working Groups
• • DSD
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  • Obesity
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  • Bone & Growth Plate
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  • Diabetes Technology
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  • Paediatric and Adolescent Gynaecology
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  • Gender Dysphoria
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  • Turner Syndrome
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  • ESPE Nursing and Allied Health Professionals
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• Endo-ERN Session
• • (1)
  • • Life Long Management of Childhood Craniopharyngioma

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• Free Communications
• • Diabetes and Insulin Session 1
  • • Insulin Resistance Leads to Mitochondrial Dysfunction in Hepatocyte

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    • Three New Genes (PTPRD, SYT9, and WSF1) Related to Korean Maturity-Onset Diabetes in the Young (MODY) Children Decrease Insulin Synthesis and Secretion in Human Pancreatic Beta Cells

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    • Next Generation Sequencing in Greek MODY Patients Increases Diagnostic Accuracy and Reveals a High Percentage of MODY12 Cases

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    • The Diabetes Drug Metformin Reverses Cognitive Impairment and Attenuates Insulin Receptor in Diabetic Aging Female Rat Brain: A Link with Diabetes and Alzheimer's Disease

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    • FADES: A Birth Cohort to Understand the Mechanisms Underlying Accelerated Onset of Autoimmunity in Children with Down's Syndrome

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    • A Novel Biochemical Marker, Fatty Acid-Binding Protein 4, in Diabetic Ketoacidosis in Children

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  • Bone, Growth Plate and Mineral Metabolism Session 1
  • • Continued Improvement in Clinical Outcomes with Burosumab, a Fully Human Anti-FGF23 Monoclonal Antibody: Results from a 3-Year, Phase 2, Clinical Trial in Children with X-Linked Hypophosphatemia (XLH)

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    • Benefits of Long-Term Burosumab Persist in 11 Girls with X-Linked Hypophosphatemia (XLH) Who Transitioned into Adolescence During the Phase 2 CL201 Trial

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    • Higher Dose of Burosumab is Needed for Treatment of Children with Severe Forms of X-Linked Hypophosphatemia

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    • New Imaging Approaches to the Quantification of Musculoskeletal Alterations in X-linked Hypophosphatemic Rickets (XLH)

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    • Age and Gender-Specific Reference Data for High-Resolution Magnetic Resonance Based Musculoskeletal Parameters in Healthy Children and Young People

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    • Validation of a New Version of BoneXpert Bone Age in Children with Congenital Adrenal Hyperplasia (CAH), Precocious Puberty (PP), Growth Hormone Deficiency (GHD), Turner Syndrome (TS), and other Short Stature Diagnoses

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  • Multi-system Endocrine Disorders
  • • Germline-Derived Gain-of-Function Variants of Gsa-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis: The First Report

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    • CFTR Loss-of-Function has Effects on microRNAs (miRNAs) that Regulate Genes Involved in Growth, Glucose Metabolism and in Fertility in in vitro Models of Cystic Fibrosis

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    • Variability in Drug Metabolizing Cytochrome P450 Activities Caused by Human Genetic Variations in NADPH Cytochrome P450 Oxidoreductase (POR)

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    • Droplet Digital PCR is a Useful Method for Detection of Mosaic Mutations in Patients with McCune-Albright Syndrome

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    • Evaluation of Endocrine Late Effects in Survivors of Childhood Allogeneic Hematopoietic Stem Cell Transplantation in Australia – Database from 1985 to 2011

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    • Severe Infections Contribute to Increased Risk of Early Death in Patients with Apeced

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  • Fat Metabolism and Obesity Session
  • • Involvement of Visfatin in Adipose Tissue Fibrosis Through Modulation of Extracellular Matrix Proteins

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    • Characterization of the Adipose Progenitor Cell Marker MSCA1 in Normal Weight and Obese Children

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    • Circulating Growth-and-Differentiation Factor-15 in Early Life: Relation to Prenatal and Postnatal Size

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    • The rs72613567:TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children

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    • Leptin Gene Methylation Status in Egyptian Infants

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    • Brain Satiety Responses to a Meal in Children Before and After Weight Management Intervention

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  • Thyroid
  • • Randomised Trial of Block and Replace Versus Dose Titration Antithyroid Drug Treatment in Children and Adolescents with Thyrotoxicosis

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    • Lower Proportion of CD19+IL-10+ and CD19+CD24hiCD27+ IL-10+, but not CD1d+CD5+CD19+CD24+CD27+ IL-10+ B Cells in Children with Autoimmune Thyroid Diseases

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    • Predominant DICER1 Mutations in Pediatric Follicular Thyroid Carcinomas

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    • Thyroid Dysgenesis: Exome-Wide Analysis Identifies Rare Variants in Genes Involved in Thyroid Development and Cancer

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    • Identification of TRPC4AP as a Novel Candidate Gene Causing Thyroid Dysgenesis

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    • Homozygous Loss-of-Function Mutation in the SLC26A7 Gene Coding a Novel Iodide Transporter Causes Goitrous Congenital Hypothyroidism

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  • Bone, Growth Plate and Mineral Metabolism Session 2
  • • Bone Tissue Characterization of a Mouse Model of Atypical Type VI Osteogenesis Imperfecta Reveals Hypermineralization of the Bone Matrix, Elevated Osteocyte Lacunardensity and Altered Vascularity

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    • Zone Wise Cell Separation Methods Comparison, Based on Relative Expression of Specific Growth Plate Markers in a Pig Model

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    • Decreased Trabecular Bone Mineral Density and Muscle Area at the Forearm Despite Improvement in Glycaemic Control Over 3 Years After Simultaneous Pancreas Kidney Transplantation

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    • Metabolically Unhealthy Obese Children and Adolescents Have Higher Bone Mineral Density Than Normal Weighted Controls but Lower than Metabolically Healthy Obeses: No Effect of FGF21 Levels

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    • No Change in Bone Density During 6 Months Off GH in Adolescents with Severe GHD at Near-Adult Height

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    • Craniosynostosis in Inactivating PTH/PTHrP Signaling Disorder 2: A Non-Classical Feature to Consider

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  • Diabetes and Insulin Session 2
  • • Deployment of a Predictive Model Based on CpG Methylation Haplotypes Analysis on the Insulin Gene Promoter, in a Cohort of Children and Adolescents with Type 1 Diabetes

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    • Copeptin Kinetics and its Relationship to Osmolality During Rehydration for Diabetic Ketoacidosis in Children: An Observational Study

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    • MicroRNA Circulating Levels in Children at Diagnosis of Type 1 Diabetes

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    • Metabolic Syndrome Features in Pre-Pubertal Children Born After Maternal Pre-Eclampsia

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    • Is the 1-hour Post-Load Glucose Level by 75g Oral Glucose Tolerance Test a New Risk Factor in Predicting Atherosclerosis?

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    • 2017 American Academy of Pediatrics Clinical Practice Guideline: Impact on Prevalence of Arterial Hypertension in Children and Adolescents with Type 1 Diabetes mellitus

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  • Pituitary, Neuroendocrinology and Puberty Session 1
  • • Hypothalamic AgRP Neurons Drive Endurance in Food-restricted Mice

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    • Analysis of Hypothalamic Metabolic Circuits after Normalization of Body Weight in Mice That Had Been Obese Due to High Fat Diet Intake

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    • Absence of Central Adrenal Insufficiency in Adults with Prader-Willi Syndrome

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    • Peripheral and Hypothalamic Alterations in the Insulin-like Growth Factor (IGF) System in Response to High Fat Diet-induced Weight Gain

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    • LGR4-Wnt β-Catenin Signalling Directs GnRH Network Development, with Defects Leading to Self-Limited Delayed Puberty

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    • Source and Changes in Serum Level of Kisspeptin in Female Rats at Different Developmental Stages

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  • Fetal, Neonatal Endocrinology and Metabolism (to include Hypoglycaemia)
  • • Using CRISPR/Cas9 Gene Editing to Study the Molecular Mechanisms of Congenital Hyperinsulinism (CHI)

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    • Heterozygous Insulin Receptor (INSR) Mutation associated with Neonatal Hyperinsulinaemic Hypoglycaemia and Familial Diabetes Mellitus

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    • DNA Methylation Signatures in Placenta and Umbilical Cord: Association with Maternal Obesity

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    • Prenatal Environment and Genetic Background Influence Urinary Steroid Excretion in Monozygotic Twins with Intra-Twin Birth-Weight Differences

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    • Iodine Status of Pregnant Women and Their Newborns in the UK – the MABY Study

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    • [18F]F-DOPA-PET/MRI or /CT in Children with Congenital Hyperinsulinism

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  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology
  • • Investigating the Roles of Androgens in Male Reproductive Development, Maintenance and Function by Characterisation of Androgen and Cortisol Deficient 11ß-Hydroxylase Mutant Zebrafish Lines

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    • The Fruit Fly, Drosophila Melanogaster, as a Model to Elucidate Human Differences of Sex Development (DSD)

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    • Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome

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    • Loss-Of-Function and Missense Mutations in MYRF are a Novel Cause of Autosomal Dominant 46,XY Leydig Cell Hypoplasia and 46,XY Gonadal Dysgenesis

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    • Transcriptome Analysis of Novel Sertoli Cell Models to Highlight Potential Genes Involved in DSD Mechanism of Disease

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    • Evaluation of Basal and GNRH-stimulated AMH Levels in Central Precocious Puberty, Peripheral Precocious Puberty and Premature Thelarche

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  • Pituitary, Neuroendocrinology and Puberty Session 2
  • • Phenotypic Characterization of a Large Pediatric Cohort of Patients with Genetic Forms of Congenital Hypopituitarism

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    • A Novel Minor Spliceosome Defect Associated with Growth Hormone Deficiency (GHD) and Primary Ovarian Insufficiency (POI)

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    • A Novel Genetic Aetiology for Familial Neonatal Central Diabetes Insipidus

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    • Whole Exome Sequencing in a Familial Case of Adamantinomatous Craniopharyngioma Revealed Two Hits Affecting Wnt-Signaling Pathway

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    • Survival, Endocrine Disorders and Quality of Life in 135 Children with Craniopharyngioma After Surgical or Combined Treatment

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    • Pubertal Timing in Parents is Associated with Timing of Pubertal Milestones in Offspring of Concordant Sex – but Only Inconsistently with Milestones in Offspring of Discordant Sex

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  • Growth and Syndromes (to include Turner Syndrome)
  • • Increasing Knowledge in IGF1R Defects: Lessons from 20 New Patients

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    • NPR2 Gene Mutations were Found in 5.4% Children with Familial Short Stature

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    • Growth Hormone Treatment in Adults with Prader-Willi Syndrome has Sustained Positive Effects on Body Composition

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    • Integration of Transcriptomic and Epigenomic Data in Childhood Identifies a Subset of Individuals Born Small for Gestational Age (SGA) with "catch-up" Growth Who Become Pre-Hypertensive in Early Adulthood

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    • Integrated Analysis of Baseline Blood Transcriptome and Genome Identifies Clusters of Turner Syndrome Patients with Different Responses to Recombinant Human Growth Hormone

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    • An Integrated Systems Biology Analysis of the Genome, Epigenome and Transcriptome Identifies a Distinct Pattern of Hypermethylation Associated with Low Childhood Growth

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  • Adrenals and HP Axis
  • • Peptide MC2R Antagonists as a New Potential Therapeutic Approach for Congenital Adrenal Hyperplasia

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    • Sexual Dimorphism in Cortisol Production and Metabolism Throughout Pubertal Development: A Longitudinal Study

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    • YAP1-HIPPO Pathway as a Novel Prognostic Marker and Therapeutic Target for Pediatric Patients with Adrenocortical Tumors (ACT)

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    • Biphasic Glucocorticoid Rhythm in One Month Old Infants: Reflection of a Developing HPA-Axis?

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    • SGPL1 Deficiency Leads to Downregulation of Key Enzymes Within the Steroidogenic Pathway

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    • Insights Into the Role of Cortisol in the Formation of the Clock/Bmal1 Complex and its Interaction with dsDNA, via Molecular Dynamics Simulations

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  • GH and IGF1
  • • Inhibition of IGF1R by IGF1R/IR Inhibitor OSI906 as a Targeted Therapy for Glioblastoma: in vitro> & in vivo Studies

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  • GH and IGF2
  • • Pubertal Onset in 1572 Girls with Short, Normal and Tall Stature: Associations to Height, Serum IGF-I and PAPP-A2 Genotypes

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  • GH and IGF3
  • • PAPP-A2 Deficiency Induces Sex-Specific Changes in Hydroxyapatite-(CaOH) Crystallinity and the Effects of IGF-1 on Bone Composition in Adult Mice

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  • GH and IGF4
  • • Once-Weekly TransCon hGH vs. Daily hGH in Pediatric Growth Hormone Deficiency: The Phase 3 heiGHt Trial

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  • GH and IGF5
  • • Once-weekly Somapacitan vs Daily Growth Hormone (Norditropin®) in Childhood Growth Hormone Deficiency: One-year Results from a Randomised Phase 2 Trial

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  • GH and IGF6
  • • Effects of 8 Years of Growth Hormone Treatment on Cognition in Children with Prader-Willi Syndrome

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  • Late Breaking Abstracts
  • • DLG2 Mutations in Patients with Delayed or Absent Puberty

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    • HDAC4 Mutations Cause Diabetes and Induce β-Cell FoxO1 Nuclear Exclusion

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    • The P450 Side-Chain Cleavage Isozyme Cyp11A2 Facilitates Interrenal and Gonadal Steroid Hormone Biosynthesis in Developing and Adult Zebrafish

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    • Defects in the GnRH Neuroendocrine Network Affect the Timing of Puberty

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    • Effects of Bifidobacterium animalis subsp. lactis on Children with Prader-Willi Syndrome: A Randomized, Double-Blind, Placebo-Controlled, Crossover Trial

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    • Leptin Influences the Down-Regulation of UCP-1 Expression in Brown Adipose Tissue During Negative Energy Balance

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• Rapid Free Communications
• • Diabetes and Insulin Session 1
  • • Low Prevalence of Maternal Microchimerism in Japanese Children with Type 1 Diabetes

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    • Gabra5 Contributes to Sexual Dimorphism in POMC Neural Activity and Glucose Metabolism

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    • The Association Between IGF-1 levels and Nonalcoholic Fatty Liver Disease (NAFLD) in Adolescents with Type 2 Diabetes

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    • Estimation of Mody Frequency and Prevalent Subtypes in Pediatric Patients by Targeted NGS

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    • Decreased Circulating Levels of MOTS-c in Individuals with Newly Diagnosed Type 1 Diabetes Children

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    • An Oral Trace Element Supplementation has a Potential Beneficial Effect on Glucose Homeostasis in Transfused Patients with β-Thalassemia Major Complicated with Diabetes Mellitus

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  • Bone, Growth Plate and Mineral Metabolism Session 1
  • • Burosumab Resulted in Better Clinical Outcomes Than Continuation with Conventional Therapy in Both Younger (1-4 Years-Old) and Older (5-12 Years-Old) Children with X-Linked Hypophosphatemia

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    • Does the Treatment with Recombinant Human Growth Hormone Improve Final Height in Patients Affected by X-Linked Hypophosphatemia?

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    • Growth Hormone Effects on Metacarpal Bone Geometry and Bone Age in Growth Hormone-Deficient Children

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    • Bone Mass and Fracture Prevalence in Childhood Brain Cancer Survivors 2, 5 or 7 Years After Off Therapy

      hrp0092rfc2.4
    • Long Term Effects of Treatment with Oxandrolone (Ox) in Addition to Growth Hormone (GH) in Girls with Turner Syndrome (TS) on Bone Mineral Density in Adulthood

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    • Impact of Pubertal Suppression on Body Composition and Bone Mineral Density in Adolescents with Gender Dysphoria

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  • Multi-system Endocrine Disorders
  • • European Registries For Rare Endocrine Conditions (EuRRECa): Results From The Pilot Phase Of The Platform For e-Reporting Of Rare Endocrine Conditions (e-REC)

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    • Factors Affecting Loss to Follow-Up for Patients with Chronic Endocrine Conditions During the Pediatric Period: A Cohort Study at a Reference Center for Rare Diseases

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    • The Founder Homozygous NR5A1 Gene Mutation p.R103Q Causes Asplenia and Severe XY-DSD and XX-DSD in a Palestinian Cohort

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    • Peripheral Glucocorticoid Metabolim May Reflect Resolution of Inflammation in Kawasaki Disease

      hrp0092rfc3.4
    • Evaluation of Endothelial Function in Childhood Standard Risk Acute Lymphoblastic Leukemia Survivors: Role of Subclinical Markers and Identification of Preventable Factors

      hrp0092rfc3.5
    • Prevalence of Endocrine Complications in Duchenne Muscular Dystrophy

      hrp0092rfc3.6
  • Fat Metabolism and Obesity Session
  • • Expression of miRNAs in Circulating Exosomes Derived from Patients with NAFLD

      hrp0092rfc4.1
    • Circulating Exosomal miRNAs in Children's Nonalcoholic Steatohepatitis and the Correlation with Serum Transaminase and Uric Acid

      hrp0092rfc4.2
    • Dysregulated Gene Expression Profile in Visceral Adipose Tissue of Juvenile Wistar Rats with Catch-Up Growth: Association with Fat Expansion and Metabolic Parameters

      hrp0092rfc4.3
    • The Novel Phosphatidylinositol-3-Kinase (PI3K) Inhibitor Alpelisib Effectively Inhibits Growth of PTEN Haploinsufficient Lipoma Cells

      hrp0092rfc4.4
    • GDF5 Increased White Adipose Tissue Thermogenesis Through p38 MAPK Signaling Pathway in Fatty Acid-binding Protein 4-GDF5 Transgenic Mice

      hrp0092rfc4.5
    • Appetite Suppressing Effects of Glucoregulatory Peptides Devoid of Nausea

      hrp0092rfc4.6
  • Thyroid
  • • Hurthle Cell Carcinoma in Childhood: Retrospective Analysis of a Large Series

      hrp0092rfc5.1
    • Ultrasound Features of Multinodular Goiter in DICER1 Syndrome

      hrp0092rfc5.2
    • Experience of Thyroid Surgery in Children with Intraoperative Neuromonitoring

      hrp0092rfc5.3
    • Thyroid Dysfunction in Patients Following Thymus Transplantation in a Tertiary Centre: A 10-Year Experience

      hrp0092rfc5.4
    • A Novel Mutation in the Thyroglobulin Gene Leading to Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant

      hrp0092rfc5.5
    • Complex Single Nucleotide Polymorphisms in SEPINA 7 Lead to TBG Deficiency

      hrp0092rfc5.6
  • Bone, Growth Plate and Mineral Metabolism Session 2
  • • EFTUD2 Gene Deficiency Disturbs Maturation of Osteoblast and Inhibits Chondrocyte Differentiation via Activated p53 Signaling

      hrp0092rfc6.1
    • High Levels of LIGHT/TNFSF14 in Prader-Willi Syndrome

      hrp0092rfc6.2
    • Increased Burden of Common Risk Alleles in Children with a Significant Fracture History

      hrp0092rfc6.3
    • Targeted Molecular Genetic Diagnosis by Next Generation Sequence Analysis Method and Investigation of Responsible Candidate Genes in Patients with Osteogenesis Imperfecta

      hrp0092rfc6.4
    • Evaluating Genotype-Phenotype Correlation using an in vitro Mutagenesis Model in Bi-Allelic Mutations Resulting in Extreme Hypophosphatasia Clinical Phenotypes

      hrp0092rfc6.5
    • Genetic Aetiology Predicts Growth Hormone (GH) Treatment Outcomes in Children Born Small-For-Gestational-Age with Persistent Short Stature (SGA-SS). Lessons from a Single-Centre Cohort

      hrp0092rfc6.6
  • Diabetes and Insulin Session 2
  • • Accuracy of Glucose Sensor Estimate of HbA1c in Children with Type 1 Diabetes

      hrp0092rfc7.1
    • β-Cell Function and Glucose Effectiveness in the Development of Impaired Fasting Glucose in Obese European Children and Adolescents

      hrp0092rfc7.2
    • Osteopontin as an Early Urinary Marker of Diabetic Nephropathy in Adolescents with Type 1 Diabetes Mellitus

      hrp0092rfc7.3
    • Handgrip Strength Correlates with Insulin Resistance and the Metabolic Syndrome in Children and Adolescents: Analysis of the Korean National Health and Nutrition Examination Survey 2014-2016

      hrp0092rfc7.4
    • Dual Diagnosis of Type 1 Diabetes and ADHD

      hrp0092rfc7.5
    • Health-Related Quality of Life and Diabetes Control in Immigrant and Italian Children and Adolescents with Type 1 Diabetes and in their Parents

      hrp0092rfc7.6
  • Pituitary, Neuroendocrinology and Puberty Session 1
  • • Trade-Off Between Olfactory Bulb and Eyeball Volume in Precocious Puberty

      hrp0092rfc8.1
    • Investigation of Imprinting Alterations in MKRN3 and DLK1 in a Cohort of Girls with Central Precocious Puberty Through Specific DNA Methylation Analysis

      hrp0092rfc8.2
    • Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5'-UTR Region of the Imprinted MKRN3 Gene

      hrp0092rfc8.3
    • Evaluation of Puberty in Patients with Noonan Syndrome and Mutations in the RAS/MAPK Genes

      hrp0092rfc8.4
    • CHD7 Mutations in Patients with Anosmic or Normosmic Idiopathic Hypogonadotropic Hypogonadism

      hrp0092rfc8.5
    • Growth, Pubertal Course and Long-Term Outcome of 46,XY Boys Born with Atypical Genitalia and Low Birthweight

      hrp0092rfc8.6
  • Fetal, Neonatal Endocrinology and Metabolism (to include Hypoglycaemia)
  • • Targeted Next-Generation Sequencing for Congenital Hypothyroidism with Positive Neonatal TSH Screening Results

      hrp0092rfc9.1
    • Age-Specific Reference Values for Plasma FT4 and TSH Concentrations in Healthy, Term Neonates at Day Three to Seven, and 13 to 15 of Life

      hrp0092rfc9.2
    • Neonatal Screening for Congenital Hypothyroidism: Analysis of a Large Coorte of Affected Patients (1987-2017) and Relationship with Perfluoroalkylated Substances (Pfas) in North-Eastern Italy

      hrp0092rfc9.3
    • Correlation Between Genotype and Phenotype Characteristics in Children with Congenital Hyperinsulinism (CHI) in a Specialist Centre

      hrp0092rfc9.4
    • Spectrum of Neuro-Developmental Disorders in Children with Congenital Hyperinsulinism Due to Activating Mutations in GLUD1

      hrp0092rfc9.5
    • Extra Uterine Growth Restriction (EUGR) in Very Low Birth Weight Infants: Growth Recovery and Neurodevelopment by the Corrected Age of 2 Years Old

      hrp0092rfc9.6
  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology
  • • Contemporary Surgical Approach in CAH 46XX – Results from the I-DSD/I-CAH Registries

      hrp0092rfc10.1
    • Cryptorchid Boys with Abrogated Mini-Puberty Display Differentially Expressed Genes Involved in Sudden Infant Death Syndrome

      hrp0092rfc10.2
    • Level of Uncertainty in Diagnostic Evaluation of Boys With XY Disorders of Sex Development (DSD)

      hrp0092rfc10.3
    • qPCR Screening for Xp21.2 Copy Number Variations in Patients with Elusive Aetiology of 46,XY DSD

      hrp0092rfc10.4
    • Variants in NWD1 Gene Leading to Different Degrees of Gonadal Dysgenesis

      hrp0092rfc10.5
    • A Mutation in the Nucleoporin-107 Gene Causes Aberrant Dpp/BMP Signaling and XX Gonadal Dysgenesis

      hrp0092rfc10.6
  • Pituitary, Neuroendocrinology and Puberty Session 2
  • • National United Kingdom Evidence- and Consensus-Based Guidelines for the Investigation, Treatment and Long-Term Follow-Up of Paediatric Craniopharyngioma

      hrp0092rfc11.1
    • Prevalence and Predicting Factors of Endocrine Dysfunction in Children with NF1 and Optic Gliomas

      hrp0092rfc11.2
    • Polycystic Ovarian Syndrome in Adolescents: Utilising Discovery Proteomics and the Search for to Identify Novel Non-Invasive Biomarkers

      hrp0092rfc11.3
    • Increased Adrenal and Testicular Androgen Concentrations Before Puberty and in Early Puberty Correlate to Adult Height Outcomes in Males with Silver-Russell Syndrome

      hrp0092rfc11.4
    • IGF-1 Serum Concentrations and Growth in Children with Congenital Leptin Deficiency (CLD) Before and After Replacement Therapy with Metreleptin

      hrp0092rfc11.5
    • Final Height Reduction in Transgender Adolescent Girls: A Case Series

      hrp0092rfc11.6
  • Growth and Syndromes (to include Turner syndrome)
  • • Karyotyping of Oocytes, Granulosa Cells and Stromal Cells in the Ovarian Tissue from Patients with Turner Syndrome: A Pilot Study

      hrp0092rfc12.1
    • Treatment with Growth Hormone Increases Klotho Concentration in Patients with Turner Syndrome

      hrp0092rfc12.2
    • Imprinting Defects and Copy Number Variations in Short Children Born Small for Gestational Age

      hrp0092rfc12.3
    • NIPBL is Required for Postnatal Growth and Neural Development

      hrp0092rfc12.4
    • Cognitive and Neuroradiological Assessments in Silver Russell Patients

      hrp0092rfc12.5
    • Exploring the Usefullness of a New Type of Pubertal Heigh Reference Based on Growth Aligned or Onset of Pubertal Growth

      hrp0092rfc12.6
  • Adrenals and HP Axis
  • • Children and Adolescents in the United States with Congenital Adrenal Hyperplasia are not at Increased Risk for Attention-Deficit/Hyperactivity Disorder

      hrp0092rfc13.1
    • Development of Novel Non-Invasive Strategies for Monitoring of Treatment Control in Patients with Congenital Adrenal Hyperplasia

      hrp0092rfc13.2
    • Establishment of Reference Intervals for Hair Cortisol in Healthy Children Aged 0-18 Years Using Mass Spectrometric Analysis

      hrp0092rfc13.3
    • Loss-Of-Function NNT Mutations Impair Antioxidants Mechanisms and Decreases Cortisol Secretion in Patients with Famililar Glucocorticoid Deficieny

      hrp0092rfc13.4
    • Genetics of Familial Glucocorticoid Deficiency Over the Decades: Phenotypic Variability and Associated Features

      hrp0092rfc13.5
    • Inhibitory Effects of Curcuminoids on the Enzymes from the Steroidogenic Pathway

      hrp0092rfc13.6
    • PAPP-A2 Deficiency Results in Sex-Dependent Modifications in Hypothalamic Regulation of Energy Homeostasis

      hrp0092rfc14.1
    • Deciphering Genetic Aetiology Among Children Born Small-For-Gestational-Age with Persistent Short Stature (SGA-SS): Phenotypic Characteristics at Diagnosis in a Large Single-Centre Cohort

      hrp0092rfc14.2
    • MicroRNAs Change and Target Key Regulatory Genes Involved in Longitudinal Growth in Patients with Idiopathic Isolated Growth Hormone Deficiency (IGHD) on Growth Hormone (GH) Treatment

      hrp0092rfc14.3
    • GHR Transcript Heterogeneity May Explain the Phenotypic Variability in Patients with Homozygous GHR Pseudoexon (6ψ) Mutation

      hrp0092rfc14.4
    • Bioactive IGF-I Concentration Compared to Total IGF-I Concentration Before and After 1 Year of High-Dose Growth Hormone in Short Children Born Small for Gestational Age - North European SGA Study (NESGAS)

      hrp0092rfc14.5
    • Growth Hormone Deficiency (GHD): Assessing Burden of Disease in Children and Adolescents: The Growth Hormone Deficiency – Child Impact Measure (GHD-CIM)

      hrp0092rfc14.6
• RFC - Late Breaking
• • Late Breaking Abstracts
  • • Preclinical Studies of Acrodysostosis Gene AAV Therapy in a Knock-In R368X PRKAR1A Mouse Model

      hrp0092rfc15.1
    • BMP4 Mutations as a Novel Cause of Normosmic Hypogonadotropic Hypogonadism

      hrp0092rfc15.2
    • Metformin Treatment Affects ACTH Receptor Activation and Downstream Signaling: A Potential Treatment for ACTH Excess Disorders and Management of Hyperandrogenic States

      hrp0092rfc15.3
    • Clinical and Genetic Characterization of 148 Patients with Persistent or Transient Congenital Hyperinsulinism: A Population-Based Study in Finns

      hrp0092rfc15.4
    • De novo Missense Mutation in SP7 in a Patient with Cranial Hyperostosis, Long Bone Fragility, and Increased Osteoblast Number

      hrp0092rfc15.5
    • Absence of Puberty and Estrogen Resistance by Estrogen Alpha Receptor Inactivation in Two Sisters: A Mutation for Variable Phenotypic Severity

      hrp0092rfc15.6
• Prize Winners
• • Development of Testicular Organoids to Understand Disorders of Sex Development
  • • Development of Testicular Organoids to Understand Disorders of Sex Development

      hrp0092ha1
  • Partial CRISPR/Cas9 IL1R1 & IFNGR1 Knock-Down Improves ß-Cell Survival and Function Under Cytokine-Induced Inflammation
  • • Partial CRISPR/Cas9 IL1R1 & IFNGR1 Knock-Down Improves β-cell Survival And Function Under Cytokine-Induced Inflammation

      hrp0092ha2
• Poster Presentations
• • Top 20 Poster
  • • Circulating miR-451a: A Biomarker to Guide Diagnosis and Treatment of Polycystic Ovary Syndrome in Adolescent Girls

      hrp0092t1
    • Assessment of ZnT8 Antigen in Thyroid Cells in Children and Adolescents with Hashimoto Thyroiditis and Nodular Goitre

      hrp0092t2
    • Hypothalamus and Pituitary Gland Antibodies in Childhood-Onset Brain Tumors and Pituitary Dysfunction

      hrp0092t3
    • Use of Stored Serum in the Study of Time Trends and Geographical Differences in Exposure of Pregnant Women to Phthalates

      hrp0092t4
    • Evaluation of Toll-like Receptor 2 Expression on T Lymphocytes in Patients with Graves' Disease in Relation to the Clinical Parameters

      hrp0092t5
    • Obesity in Pediatric Age: The Analysis of Genomic Rearrangements

      hrp0092t6
    • Establishing of a Novel NGS Tool for the Diagnosis of X-linked Hypophosphatemia (XLH)

      hrp0092t7
    • Bone Mineral Density (BMD) in Women with Turner Syndrome (TS) from the DSD-LIFE Cohort, an Epidemiological Study

      hrp0092t8
    • Empagliflozin and GABA Improve β-Cell Mass and Glucose Tolerance in New-Onset Type 1 Diabetes

      hrp0092t9
    • Changes in Adrenal Androgens and Steroidogenic Enzyme Activities in Children Aged 2, 4, and 6 Years: Steroid Hormone Profiling From the Prospective Cohort Study

      hrp0092t10
    • Droplet Digital PCR Techniques to Detect R201 Mutations in the Mccune-Albright Syndrome

      hrp0092t11
    • The First Description of Large Pathogenic Deletion in ACAN Gene and Additional Cases with Novel Pathogenic ACAN Variants

      hrp0092t12
    • Results from the Implementation of a 2 Year Growth Awareness and Growth Disorders Screening Campaign (GrowInform)

      hrp0092t13
    • The Effect of Endocine Disrupting Chemicals to Precocious Puberty in Children with Exposure History of 'Slim'

      hrp0092t14
    • Intestinal Microbiota Development Differs Between Pubertal Boys and Girls

      hrp0092t15
    • IGF2 Mutations: Report of Six Japanese Cases and Phenotypic Comparison with H19/IGF2:IG-DMR Epimutations Including Literature Cases

      hrp0092t16
    • Factors Associated with Dyslipidemia in Patients with Type 1 Diabetes: A Single-Center Experience

      hrp0092t17
    • Early Treatment with Intravenous Bisphosphonates Prevents Severe Postnatal Bone Loss in Children with Osteogenesis Imperfecta

      hrp0092t18
    • Urinary Gonadotrophins in Girls with Turner Syndrome

      hrp0092t19
    • Molecular and Phenotypic Spectrum of Noonan Syndrome in Chinese Patients

      hrp0092t20
• Poster Category 1
• • Adrenals and HPA Axis
  • • Could a Glucocorticoid Receptor Polymorphism be Protective against Hypothalamic-Pituitary-Adrenal Axis Suppression in Asthmatic Children on Corticosteroids?

      hrp0092p1-1
    • Software-assisted Analysis of the Urinary Steroid Metabolom in Treated Children with Classic Congenital Adrenal Hyperplasia

      hrp0092p1-2
    • Simplifying the Interpretation of Steroid Metabolome Data by a Machine-Learning Approach

      hrp0092p1-3
    • The Steroidal Milieu in Amniotic Fluid of Mid-Gestation: A Targeted GC-MS Metabolomics Study

      hrp0092p1-4
    • 18 years of neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: recall rate reduction thanks to liquid chromatograpy-tandem mass spectrometry as second tier test

      hrp0092p1-5
    • Health status of children with Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency in the United Kingdom: results of a multi-centre cohort study

      hrp0092p1-6
    • Influence of Internal Standards Choice on Quantification of 17α-hydroxyprogesterone (17OHP) Using Mass Spectrometric Based Methods

      hrp0092p1-7
    • Follow-up and Prevalence of Precocious Puberty in Children with Classical Congenital Adrenal Hyperplasia diagnosed by Neonatal Screening

      hrp0092p1-8
    • A Simulation-based Intervention Teaching Illness Management Skills to Caregivers of Children with Adrenal Insufficiency: a Randomised Controlled Study

      hrp0092p1-9
    • Global Practice of Glucocorticoid and Mineralocorticoid Treatment in Children and Adults with Congenital Adrenal Hyperplasia – Insights from the I-CAH Registry

      hrp0092p1-10
    • Assessment of the Adrenal Function in Children with Acute Lymphoblastic Leukemia Before and After Induction Therapy with Corticosteroids

      hrp0092p1-11
    • Trientine Treatment Mimicking Severe Hyperandrogenism

      hrp0092p1-12
    • Cytokines and the Impairment of Puberty

      hrp0092p1-13
  • Bone, Growth Plate and Mineral Metabolism
  • • Refractory Hypercalcemia After Denosumab Treatment in Pediatric Age: A Case Report

      hrp0092p1-14
    • The Overweight and Obesity Decrease the Growth Potential in Mexican Children and Adolescents

      hrp0092p1-15
    • Normocalcemic Hyperparathyroidism in Children

      hrp0092p1-16
    • Serum Testosterone Level at the Age of 12 is an Important Determinant of the Following Gain of Bone Mineral Apparant Density in 18-year Old Males: a Longitudinal Study From Puberty

      hrp0092p1-17
    • Nephrocalcinosis in Children with X-Linked Hypophosphatemia: Prevalence and Risks Factors

      hrp0092p1-18
    • Effects of Punica Granatum (Pomegranate) Seed Oil Extract on Bone Turnover and Resorption Induced in Ovariectomized Rats

      hrp0092p1-19
    • Long-term Teriparatide (rhPTH) Treatment in Children with Syndromic Hypoparathyroidism

      hrp0092p1-20
    • Dual X-ray Absorptiometry in Children With Hypophosphatasia Treated with Asfotase Alfa: A Pooled Post Hoc Analysis

      hrp0092p1-21
    • Differences in Bone Strength and Cortical Bone Parameters in Young Swedish Women with Type 1 Diabetes

      hrp0092p1-22
    • Increased Prevalence of Overweight and Obesity and its Clinical Predictors in Children Affected by X-Linked Hypophosphatemia

      hrp0092p1-23
    • Novel Homozygous LRP5 Mutations in Patients with Osteoporosis-Pseudoglioma Syndrome

      hrp0092p1-24
  • Diabetes and Insulin
  • • Pathogenicity of GCK Gene Mutation c.364C>G (p.Leu122Val)

      hrp0092p1-25
    • Myocardial Function in Asymptomatic Children with Type 1 Diabetes

      hrp0092p1-26
    • A Case of Neonatal Diabetes with Hyperferritinemia: A Distal PTF1A Enhancer Mutation

      hrp0092p1-27
    • Elevated Anti-tissue Transglutaminase Antibodies in Children Newly Diagnosed with type 1 Diabetes do not Always Indicate Celiac Disease

      hrp0092p1-28
    • What Hypoglycemia Does to the Heart: Impact of Nocturnal Hypoglycemia on Cardiac Repolarization in Diabetic Children

      hrp0092p1-29
    • Effects of Glypican-4 Protein on INS1E Cell Viability and Insulin Signalling

      hrp0092p1-30
    • Dual Diagnosis of Type 1 Diabetes and ADHD

      hrp0092p1-31
    • Heterozygous RFX6 Mutation as a Cause of Diabetes Mellitus in a Multigenerational Family

      hrp0092p1-32
    • Plasma Tocopherols and Carotenes are Decreased in Spanish Children and Adolescents with Insulin Resistance, Independently of Obesity

      hrp0092p1-33
    • Serum Dipeptidyl peptidase-4 Activity and its Relation to Insulin Resistance in Type 1 Diabetic Adolescents

      hrp0092p1-34
    • The Impact of CGM Availability: Real World Data From a Population Based Clinic

      hrp0092p1-35
    • Expression of Receptor for Advanced Glycation End-products and its Ligands HMGB1 and s100A12 in Children and Adolescents with New-onset Type 1 Diabetes and in Patients with Longer Disease Duration

      hrp0092p1-36
    • Association of Maternal Depressive Symptoms with Worse Metabolic Control in Adolescents with Type 1 Diabetes

      hrp0092p1-37
    • The Factors Associated with High Levels of HbA1C in Children and Young People with Type 1 Diabetes Mellitus

      hrp0092p1-38
  • Fat, Metabolism and Obesity
  • • Differences Between Short- and Long-term Outcomes of Laparoscopic Sleeve Gastrectomy in Adolescence

      hrp0092p1-39
    • Late Pregnancy Exposure to Mono(2-ethyl-5-hydroxyhexyl) Phthalate Affects Weight Z-scores in Children up to 2 Years

      hrp0092p1-40
    • Growth Arrest-Specific 6 (Gas6) Protein is Associated with Adiposity and Metabolic Syndrome in Obese Children and Adolescents

      hrp0092p1-41
    • De-novo and Depot-Specific Androgen Production in Human Adipose Tissue - a Source of Hyperandrogenism in Obese Females

      hrp0092p1-42
    • Association of Biomarkers of Endothelial Dysfunction with MicroRNAs Levels in Overweight and Obese Adolescentes

      hrp0092p1-43
    • Metabolic Complications After Paediatric Liver Transplantation: A 10-year Longitudinal Study in a South-East Asian Population

      hrp0092p1-44
    • Non-Alcoholic Fatty Liver Disease and eGFR Levels could be Linked by the PNPLA3 I148M Polymorphism in Obese Children

      hrp0092p1-45
    • How to Recognize Underlying Somatic Causes of Paediatric Obesity? Performance of the Diagnostic Recommendations of the Endocrine Society Guideline and Suggestions for Improvement

      hrp0092p1-46
    • How Early is 'extreme Early-Onset Obesity'? Results of Comprehensive Growth Curve Analysis to Identify Genetic Obesity Disorders Based on Age of Onset of Obesity

      hrp0092p1-47
    • Waist Circumference Triglyceride Index is Useful to Predict Non-alcoholic Fatty Liver Disease in Childhood Obesity

      hrp0092p1-48
    • Gut Microbiome of North-American Children with and without Prader-Willi Syndrome (PWS)

      hrp0092p1-49
    • Two-year Outcomes of Whanau Pakari: A Novel Home-based Intervention for Child and Adolescent Obesity

      hrp0092p1-50
    • Pathogenic Mutations and Variants in KSR2 in a Cohort of Obese Children

      hrp0092p1-51
    • Effect of Feeding Mode on Longitudinal Body Composition in Early Life

      hrp0092p1-52
    • Age of Obesity Onset could be the First Indicator of Future Metabolic Complications – Preliminary Data of Prospective Multicenter Study

      hrp0092p1-53
    • Augmented Fibroblast Growth Factor 21 Serum Levels in Metabolic Disorders and Association With Endothelial Function in Childhood

      hrp0092p1-54
    • A Novel Recurrent Heterozygous Plin1 Mutation in Three Russian Patients with Partial Lipodystrophy, Dyslipidemia and Insulin Resistance

      hrp0092p1-55
    • Carotid Intima-Media Thickness Relates Rather to Epicardial and Perirenal Fat than Total Body Adiposity in Apparently Healthy Children

      hrp0092p1-56
    • Put Your Money Where Your Mouth is: Preliminary Evidence that Oral Microbiota Diversity may Shape Later Cardiometabolic Health in Children

      hrp0092p1-57
    • A Case-Control Study of Exposure to Bisphenol-a and Phthalates in Obese Children

      hrp0092p1-58
    • Growth Patterns in Non-syndromic Childhood Overweight: Comparing Children with Early of Late Onset Weight Gain

      hrp0092p1-59
    • The Effect of Improved Metabolic Risk Factors and Metformin Therapy on Circulating Hepatokines in Obese, Insulin-Resistant Adolescents

      hrp0092p1-60
    • Association Among PGRN, HMGB1, and Obesity Related Markers in Young Rat Model of High Fat Diet-Induced Obesity

      hrp0092p1-61
    • Short-term Treatment of Liraglutide in Patient with Prader-Willi Syndrome

      hrp0092p1-62
    • Altered Gut Microbiota in Obese Children: Sex-associated Signature

      hrp0092p1-63
  • Fetal, Neonatal Endocrinology and Metabolism (to include Hypoglycaemia)
  • • Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome

      hrp0092p1-64
    • Congenital Hyperinsulinism Due to Pancreatic Mosaicism for Paternal Uniparental Disomy of all Chromosome 11, with the Additional Finding of Pancreatic Mosaicism for Trisomy 12

      hrp0092p1-65
    • Diagnostical Approach to Adrenal Failure in Symptomatical Preterm Infants – is Saliva Derived Free Cortisol the Solution?

      hrp0092p1-66
    • Screening of Congenital Hypothyroidism using Umbilical Cord Blood in a Maternity Hospital

      hrp0092p1-67
    • Growth and Cognition at Peri-Pubertal Age in Preterm Infants Very Low Birth Weight: The Role of Extrauterine Growth Restriction (EUGR)

      hrp0092p1-68
    • Molecular Mechanisms of Idiopathic Ketotic Hypoglycemia in Children

      hrp0092p1-69
    • Congenital Hypothyroidism – Precise Diagnosis with Dual Imaging

      hrp0092p1-70
    • Clinical, Biochemical and Echocardiographic Evaluation of Patients with Congenital Rickets Due to Maternal Vitamin D Deficiency

      hrp0092p1-71
  • GH and IGFs
  • • Diagnostic Value of Random Serum Growth Hormone (GH), IGF-I and IGFBP-3 Concentrations for the Diagnosis of Growth Hormone Deficiency (GHD) in Patients Below One Year of Life

      hrp0092p1-72
    • Influence of Birth Parameters on Growth Response and Metabolic Effects of Growth Hormone (GH) Therapy in GH-deficient Children and Adolescents

      hrp0092p1-73
    • Recombinant GH Treatment in Child with Pseudopseudohypoparathyroidism Associated with Growth Hormone Deficiency

      hrp0092p1-74
    • Impact of -202 IGFBP-3 Promoter Polymorphism on Growth Responses in Korean Children with Idiopathic Short Stature

      hrp0092p1-75
    • The Diagnostic Value of Serum Acid-labile Subunit (ALS) Alone and in Combination with IGF-1 and IGFBP-3 in the Diagnosis of Idiopathic Growth Hormone Deficiency (iGHD)

      hrp0092p1-76
    • Severe IGF-I Deficiency in Children with Normal Growth Hormone (GH) Secretion and Excluded GH Insensitivity – is it Really Idiopathic Short Stature?

      hrp0092p1-77
    • Premature Infants Born Small by Gestational Age: the Role of Insulin-like Growth Factor-1 in the Regulation of Postnatal Growth

      hrp0092p1-78
    • The experience of Pain in Children with Growth Hormone Deficiency and Psychosocial Correlates: Preliminary Data from a Longitudinal Prospective Study

      hrp0092p1-79
    • Clinical Characteristics, Puberty Pattern and Adult or Near-adult-height Data in a Group of Patients with Growth Failure due to Severe Primary IGF-1 Deficiency (GROWPATI Study)

      hrp0092p1-80
    • Effect of Recombinant Growth Hormone Therapy on Retinal Nerve Fiber in Children with Idiopathic Growth Hormone Deficiency

      hrp0092p1-81
    • Positive Impact on Adherence Through Educational Activities of the Argentina´s Patient Support Program in Children with low Adherence to Treatment with Recombinant Growth Hormone (easypod applicator)

      hrp0092p1-82
    • Identification of Novel Recessive IGFALS Mutations and INSR Variant in an Obese Korean Boy

      hrp0092p1-83
  • Growth and Syndromes (to include Turner Syndrome)
  • • Development of a Parent Experience Measure for Parents of Children with Achondroplasia

      hrp0092p1-84
    • Bone Mineral Density is Normal in Prepubertal Patients with Turner Syndrome when Corrected by Height/age

      hrp0092p1-85
    • Extreme Short Stature and Poor Pubertal Growth: When FBN1 is the Culprit

      hrp0092p1-86
    • Long-Term Safety Follow-up after Omnitrope® (recombinant human growth hormone) Treatment in Short Children Born Small for Gestational Age (SGA): Latest Results

      hrp0092p1-87
    • Etiology of Severe Short Stature: Single Center Experience

      hrp0092p1-88
    • Clinical Outcomes in Primary Empty Sella (ES) Syndrome in Childhood-Onset Growth Hormone Deficiency: Data from KIGS (Pfizer International Growth Database)

      hrp0092p1-89
    • Quality of Life in Caregivers of Young Children with Prader-Willi Syndrome

      hrp0092p1-90
    • Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Panhypopituitarism Due to a Novel Heterozygous IVS11-2AC(c.1957-2AC) Mutation in GLI2 Gene

      hrp0092p1-91
    • A Rare Case of Pseudoisodicentric X Chromosome in a Patient with Primary Amenorrhoea

      hrp0092p1-92
    • Persisting Embryonal Infundibular Recess in a Patient with Morning Glory Syndrome and Multiple Pituitary Deficiencies

      hrp0092p1-93
    • Familial Occurrence of Turner Syndrome in two Tunisian Families

      hrp0092p1-94
    • The role of Physical Activity on Postural Stability and Fitness Characteristics in Pediatric Patients with GH Deficiency

      hrp0092p1-95
    • Assessment of Subjective and Objective Compliance to Growth Hormone Therapy of Children with Growth Hormone Deficiency

      hrp0092p1-96
  • Pituitary, Neuroendocrinology and Puberty
  • • Familial Neurohypophyseal Diabetes Insipidus and 2 Novel Vasopressin Gene Mutations in 13 Italian Kindreds.

      hrp0092p1-97
    • Final Height in Oncological Growth Hormone Deficient (GHD) Children After Growth Hormone (GH) Therapy

      hrp0092p1-98
    • Eating Behavior and Oxytocin in Childhood-onset Craniopharyngioma Patients: An Exploratory Study

      hrp0092p1-99
    • RNPC3 Mutations Associate Prolactin Deficiency and Ovarian Insufficiency, Expanding the Phenotype Beyond Isolated Growth Hormone Deficiency Type V (MIM#618860)

      hrp0092p1-100
    • Identification of Novel Mutations in FGFR1 and Functional Characteristics in Patients with Isolated Gonadotropin-Releasing Hormone Deficiency

      hrp0092p1-101
    • Clinical Presentation, Management, and the Outcomes of Pituitary Adenomas in Children

      hrp0092p1-102
    • A Case of Panhipopituitarism with SOX3 Gene Deletion

      hrp0092p1-103
    • Interesting Genotype-Phenotype Differences in Siblings with Familial Hypopituitarism and Pituitary Hypoplasia

      hrp0092p1-104
    • Familial Central Precocious Puberty Caused by a Novel MKRN3 Mutation

      hrp0092p1-105
    • Management and Treatment Outcome of Craniopharyngiomas in Young Children Before 4 Years of Age in Italy: Multicentre Collection of 16 Cases

      hrp0092p1-106
    • Secular Trend of Age at Menarche and Stature in Tuscan Girls: A Retrospective Study in The Birth Cohort 1995-2003

      hrp0092p1-107
    • Hyperprolactinemia in Children with Juvenile Idiopathic Arthritis

      hrp0092p1-108
    • A NCOA5 Gene Variant in A Pedigree With Maternally Inherited Precocious Puberty

      hrp0092p1-109
    • References for Testicular Volume Measured by Ultrasound and for Pubic Hair in 6-16 Year-Old Norwegian Boys

      hrp0092p1-110
    • PROKR2 in Girls with Idiopathic Central Precocious Puberty

      hrp0092p1-111
    • The Relationship between the Olfactory Bulb and Precocious Puberty:From Nose to Pituitary

      hrp0092p1-112
    • Delayed Puberty in A 16-Year-Old Male Associated with Gamma Aminobutyric Acid Capsule Supplements

      hrp0092p1-113
    • Obesity in Boys is Not Associated with Delayed Pubertal Onset

      hrp0092p1-114
    • Mutation Screening of the Sonic Hedgehog Signaling-Related Genes in 120 Japanese Patients with Congenital Hypopituitarism

      hrp0092p1-115
    • How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty

      hrp0092p1-116
    • The Role of Rat Hypothalamus Kisspeptin, Neurokinin and their respective Receptors in the Prolactin-Infertility Interaction

      hrp0092p1-117
    • Whole Exome Sequencing (WES) Reveals Oligogenic Gene Mutations in a Case of Combined Pituitary Hormone Deficiency (CPHD)

      hrp0092p1-118
    • Menarche and its Relation to the Pubertal Growth Spurt

      hrp0092p1-119
    • Role of Priming in Peri-Pubertal Growth Delays: Preliminary Results of A Large Multicenter Study

      hrp0092p1-120
  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology
  • • Lower Urinary Tract Dysfunction and Infection in Girls with Disorders of Sex Development and Urogenital Sinus

      hrp0092p1-121
    • Phenotypic, Genotypic and Biochemical Characterization Of 5 Alpha Reductase 2 Deficiency: A Pediatric Cohort From India

      hrp0092p1-122
    • Does the Internet Provide Accurate and Valid Health Information Regarding Disorders of Sex Development?

      hrp0092p1-123
    • A Human Model Showing the Ability of Testis XX Cells to Masculinise into Sertoli Cells and Success of Microtese Surgery in Paediatric Azoospermia

      hrp0092p1-124
    • A Health-Related Quality of Life Tool for Parents of Young Children With Disorders of Sex Development

      hrp0092p1-125
    • Longitudinal Changes in External Masculinisation Scores in Boys with XY Disorder of Sex Development (DSD)

      hrp0092p1-126
    • Mutations in CBX2 Associated with Gonadal Anomalies in 46,XY and 46,XX Individuals

      hrp0092p1-127
    • The Novel Founder Homozygous V225M Mutation in the 17HSDB3 Gene Causes Aberrant Splicing and Severe XY-DSD

      hrp0092p1-128
    • Molecular Diagnosis of Patients with 46,XY Differences in Sex Development in A Single Tertiary Center

      hrp0092p1-129
    • In vivo and In vitro Study of 17β Estradiol Against Amyloid Beta Neurotoxicity in Synaptosomes of Aging Female Rats: A Therapeutic Potential Drug for Parkinson's Disease

      hrp0092p1-130
    • Is there the Relationship Between Anxiety and Depression Level and Clinical Presentation of Polycystic Ovary Syndrome in Adolescent Girls?

      hrp0092p1-131
    • What is the Recurrence Rate of Benign Ovarian Tumors in Childhood? Ovarian Benign Organic Tumors (OBT) are a Rare Pathology in Childhood that Require Conservative Surgery with an Unknown Risk of Recurrence

      hrp0092p1-132
    • Congenital Disorders of Reproductive Hormones in Mini-puberty Boys with Bilateral Cryptorchidism

      hrp0092p1-133
    • Targeted Panel Gene Sequencing for Identification of Genetic Etiology of 46,XY Disorders of Sex Development

      hrp0092p1-134
    • Combining Clinical and Genetic Approaches in Diagnosing a Large Brazilian Cohort of Patients with 46,XY Differences of Sex Development (DSD)

      hrp0092p1-135
    • Serum Estradiol is Associated with Inhibin B in Healthy 1-6 Years Old Girls

      hrp0092p1-136
    • Brain MRI Findings in Girls with Central Precocious Puberty in Taiwan: One Medical Center Experience

      hrp0092p1-137
    • Changes in Body Mass Index in Boys with Central Precocious Puberty During and After Gonadotropin-Releasing Hormone Agonist Treatment

      hrp0092p1-138
    • Gonadal Function of Female Patients with Noonan Syndrome

      hrp0092p1-139
    • Methylation Status of X Inactivation-Escape Genes in Controls and Females with X Chromosome Rearrangements

      hrp0092p1-140
    • Diagnostic Value of Anti-Mullerian Hormone Level in Adolescent Females with Polycystic Ovary Syndrome

      hrp0092p1-141
    • Disorders of Sex Development (DSD): Inconsistencies Between Clinical Features and Peripheral Blood Cultured Karyotypes

      hrp0092p1-142
  • Thyroid
  • • Biotine interference in a patient with non-clinic high thyroid hormone levels

      hrp0092p1-143
    • Investigation of Iodine Deficiency in the North of Siberia

      hrp0092p1-144
    • The Investigation of Genetic Etiology in Familial Cases with Congenital Hypothyroidism

      hrp0092p1-145
    • Is There Any Correlation Between Thyroid Function Test on First Day of Admission in Critically Ill Children and Disease Severity or Outcome?

      hrp0092p1-146
    • Intrathyroidal Ectopia of Thymus in Children: Frequency, Ultrasound, Evolution

      hrp0092p1-147
    • Activating Mutation M453V in Receptor TSHR as a Cause Familial Hyperthyroidism

      hrp0092p1-148
    • Central Hypothyreoidism with Pituitary Enlargement and No Gene Alterations

      hrp0092p1-149
    • Acquired Von Willebrand's Syndrome Caused by Primary Hypothyroidism in a 5-Year-Old Girl

      hrp0092p1-150
    • Iodine Status in Newborns and Mothers in Georgia

      hrp0092p1-151
    • Thyroid Function Following Hemithyroidectomy in a Pediatric Cohort

      hrp0092p1-152
    • Homozygous c.2422delT hTPO Mutation in Three Patients with Congenital Hypothyroidism Followed Over 20 Years

      hrp0092p1-153
    • Association of Hashimoto's Thyroiditis with Antistreptolysin O titer

      hrp0092p1-154
    • Congenital Hypothyroidism Newborn Profile After a Lower TSH Cutoff for Neonatal Screening in Southern Brazil

      hrp0092p1-155
  • Adrenals and HPA Axis (1)
  • • Prospective, Open-Label, Long-Term Follow-Up of Neonates and Young Children with Adrenal Insufficiency Treated with Hydrocortisone Granules

      hrp0092p1-156
    • Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry

      hrp0092p1-157
    • Influence of Internal Standards Choice on Quantification of 17α-hydroxyprogesterone (17OHP) Using Mass Spectrometric Based Methods

      hrp0092p1-158
    • Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency

      hrp0092p1-159
    • Serum fetuin-A and insulin levels in classic congenital adrenal hyperplasia

      hrp0092p1-160
    • Perioperative Control of Blood Pressure in a Child with Paraganglioma Using Esmolol

      hrp0092p1-161
    • Evaluation of Molecular Characteristics and Steroid Metabolomics in a Large Cohort of Children with 3β-Hydroxysteroid Dehydrogenase 2 Deficiency

      hrp0092p1-162
    • "Help My Baby Cries!" Hair Cortisol as Marker for Parental Stress in Excessive Crying Infants

      hrp0092p1-163
    • The Urinary Steroid Signature of Premature Adrenarche

      hrp0092p1-164
    • How the Level of Antibodies Against 21-Hydroxylase Changes with Time in Patients with Addison's Disease

      hrp0092p1-165
    • Cortisol levels in glucagon stimulation tests in children evaluating for short stature: clinical and laboratorial correlations

      hrp0092p1-166
    • Development of an International Benchmark for Sick Day Episodes as a Core Clinical Outcome in People with Congenital Adrenal Hyperplasia

      hrp0092p1-167
  • Bone, Growth Plate and Mineral Metabolism (1)
  • • Genotype-Phenotype Characteristics in Four Families of Type II Collagenopathy in Our Hospital

      hrp0092p1-168
    • Hypercalcemia as a Post Stem Cell Transplantation Complication in Children with Osteopetrosis - A Single Centre Experience

      hrp0092p1-169
    • Efficacy and Safety of Denosumab Treatment in a Boy with Cherubism

      hrp0092p1-170
    • Evaluation of Bone Health in Adolescents and Young Adults After Allogeneic Human Stem Cell Transplantation in Childhood: A Single Center Cross-Sectional Study

      hrp0092p1-171
    • Is Serum Alkaline Phosphatase Useful in Assessing Rickets Severity on Radiographs in Children with X-Linked Hypophosphataemia on Conventional Therapy?

      hrp0092p1-172
    • Cutoff Value for 25 Hydroxy-Vitamin D Which Leading to sYmptomatic Vitamin D Deficiency in Children is 15 ng/mL in a Chemiluminescent Immunoassay

      hrp0092p1-173
    • The Optimal Dosage of Vitamin D Supplement for Vitamin D deficiency in Korean Children and Adolescents

      hrp0092p1-174
    • Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

      hrp0092p1-175
    • Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA

      hrp0092p1-176
    • Severe Hypocalcaemia in Propionic Acidaemia caused by Parathyroid Hormone Resistance and treated with Alfacalcidol

      hrp0092p1-177
  • Diabetes and Insulin (1)
  • • The Efficacy and Safety of Predictive Low Glucose Suspend Feature in Decreasing Hypoglycemia in Children with Type 1 Diabetes Mellitus: A Systematic Review and Meta-Analysis

      hrp0092p1-178
    • Longitudinal Metabolic Control After Initiation of Insulin Pump in 5,040 Pediatric Type-1-Diabetes Subjects – Heterogeneous HbA1c Trajectories Over Three Years from the DPV Registry

      hrp0092p1-179
    • Efficacy and Safety of Insulin Degludec as a Basal Insulin in Adolescents with Type 1 Diabetes During Ramadan Fasting: A Single Center Observational Study with Freestyle Libre Flash Glucose Monitoring System

      hrp0092p1-180
    • A Case of Prohormone Convertase Deficiency Diagnosed with Type 2 Diabetes Mellitus

      hrp0092p1-181
    • The Influence of Excess Iron on Pancreatic Beta Cells

      hrp0092p1-182
    • Study on the Mechanism of Metformin in Improving PGRN-Induced Insulin Resistance of 3T3-L1 Cell

      hrp0092p1-183
    • A Case with Monogenic Diabetes Caused by RFX6 Mutation in a 14-Year-Old-Girl

      hrp0092p1-184
    • Endothelial and Heart Dysfunction in Children and Adolescents with Type 1 Diabetes

      hrp0092p1-185
    • Efficacy of Autologous Hematopoietic Stem Cell Transplantation in the Treatment of Childhood Type 1 Diabetes

      hrp0092p1-186
    • Course of Puberty and Growth Spurt in Boys with Type 1 Diabetes

      hrp0092p1-187
    • A Novel Mutation in the Pancreatic Duodenal Homeobox-1(PDX-1) Gene in a Palestinian Family Resulting in Neonatal Diabetes Associated with Congenital Adrenal Hyperplasia

      hrp0092p1-188
    • A Novel SLC2A2 Mutation Implicated in Fanconi Bickel Syndrome and Dysglycemia

      hrp0092p1-189
    • Periodontal Disease Relates to Diabetes Control in Children and Adolescents with Type 1 Diabetes

      hrp0092p1-190
  • Fat, Metabolism and Obesity (1)
  • • Effect of Probiotics Intake on Obese Children

      hrp0092p1-191
    • Changes in Objectively Measured Sleep Quality After an Integral Intervention in Patients with Abdominal Obesity

      hrp0092p1-192
    • Circulating Insulin-Like Growth Factor-I Independently Predicts Blood Pressure in Apparently Healthy Children

      hrp0092p1-193
    • Whole Exome Sequencing to Identify Causative Variants in a Female Patient with Early Onset Obesity and Intellectual Disability: A New Case of Borjeson-Forsman-Lehmann syndrome

      hrp0092p1-194
    • Serum Leptin, Adiponectin and Insulin-Like Growth Factor I During Infancy were Associated with Markers of Metabolic Syndrome at Six Years of Age

      hrp0092p1-195
    • Why are Patients with Obesity Due to Leptin Receptor Deficiency not Sufficiently Recognized? Prevalence Estimation Based on European Allele Frequencies and Thoughts on the Discrepancy

      hrp0092p1-196
    • You are What You Eat: Preliminary Evidence of Associations Between Dietary Habits and Oral Microbiota Composition in Early Childhood

      hrp0092p1-197
    • Correlation of Serum Chemerin Concentrations with Obesity/Metabolic Syndrome Characteristics in Pre-Adolescents and Adolescents

      hrp0092p1-198
    • Non-Alcoholic Fatty Liver Youth with Obesity

      hrp0092p1-199
    • Ferritin, an Indicator for Inflammation or Iron Storage in Obese Children?

      hrp0092p1-200
    • Serum Kisspeptin in Obese Children and its Relation to Glucose Metabolism

      hrp0092p1-201
    • Visceral Adiposity Index as a Marker of Metabolic Risk in Survivors of Paediatric Hematopoietic Stem Cell Transplantation After Chemotherapy-Only Conditioning

      hrp0092p1-202
    • Serum Nonylphenol and Obesity in Children and Adolescents

      hrp0092p1-203
  • Fetal, Neonatal Endocrinology and Metabolism (to include Hypoglycaemia) (1)
  • • Risk Factors for Brain Injury After Transient or Persistent Hyperinsulinemic Hypoglycemia in Neonates

      hrp0092p1-204
    • Central Hypoventilation Syndrome and Hyperinsulinameic Hypoglycaemia

      hrp0092p1-205
    • Unusual Congenital Hyperinsulinism Case in a Patient with a Pathogenic GCK Mutation

      hrp0092p1-206
    • Clinical Characteristics and Long Term Follow Up of 17 Patients with Permanent Neonatal Diabetes due to PTF1A Distal Enhancer Mutations

      hrp0092p1-207
    • Transient Gonadal Activation and Infant Growth Velocity

      hrp0092p1-208
    • Urogenital Abnormalities in Children Conceived by Assisted Reproductive Technologies

      hrp0092p1-209
    • Subcutaneous Fat Necrosis of the Newborn: A Systematic Review of the Literature

      hrp0092p1-210
    • Characteristics of Children with Kabuki Syndrome and Hyperinsulinemic Hypoglycemia

      hrp0092p1-211
  • GH and IGFs (1)
  • • Hypoglycaemia Adverse Events in SPIGFD: Association with Patient Diagnosis, Age, Time-Course and Dosage of Mecasermin: 10-year Data from the European Increlex® Growth Forum Database in Europe (EU-IGFD)

      hrp0092p1-212
    • Determinants of Final Height in Patients Born Small for Gestational Age Treated with Recombinant Growth Hormone

      hrp0092p1-213
    • The European Increlex® Growth Forum Database (EU-IGFD) Registry: Do Treatment Practices Differ Between European Countries?

      hrp0092p1-214
    • Acromesomelic Dysplasia, Type Maroteaux (AMDM): Impact of Long-term (8 years) High-dose Growth Hormone Treatment on Growth Velocity and Final Height in Two Siblings

      hrp0092p1-215
    • Birth Anthropometry with Cord Blood Insulin-Like Growth Factor 1 and Leptin in Korean Appropriate-For-Gestational-Age Infants Born at ≥28 Weeks' Gestation

      hrp0092p1-216
    • Association Between Nonalcoholic Fatty Liver Disease and Growth Hormone Deficiency in Patients with Childhood-Onset Hypopituitarism

      hrp0092p1-217
    • Lessons From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion, Illustrating the Roles of IGF2 and IGF1R in Growth Regulation

      hrp0092p1-218
    • The Therapeutic Effect of A Traditional Chinese Medicine Mixture in Rat Models with Precocious Puberty Through Lin28/Let7 Pathway

      hrp0092p1-219
    • Real-World Data From Electronic Monitoring of Adherence to Growth Hormone Treatment in Children with Growth Disorders: A Descriptive Analysis

      hrp0092p1-220
    • Individual Patterns of Objectively Measured Adherence to Growth Hormone Treatment and its Effect on Growth in Prepubertal Children with Growth Hormone Deficiency

      hrp0092p1-221
    • A Patient with a Novel Homozygous Mutation in IGF1-R Gene and Response to Growth Hormone Therapy

      hrp0092p1-222
  • Growth and Syndromes (to include Turner Syndrome) (1)
  • • Tall Stature and Macrodactyly of the Great Toes Due to a Novel Mutation in the Natriuretic Peptide Receptor-2 Gene

      hrp0092p1-223
    • The Efficacy and Adverse Reactions of the Letrozole or Gonadotropin Releasing Hormone Analog Combined with Recombinant Human Growth Hormone in Short Pubertal Boys

      hrp0092p1-224
    • The Phenotypic Spectrum of Kabuki Syndrome in Patients of Chinese Descent

      hrp0092p1-225
    • Response to Growth Hormone in Very Young Children (® International Outcome Study and ANSWER Program

      hrp0092p1-226
    • Latest Results From PATRO Children, a Multi-Centre, Observational Study of the Long-Term Safety and Effectiveness of Omnitrope® in Children Requiring Growth Hormone Treatment

      hrp0092p1-227
    • Broadening of the Phenotypic Spectrum of Coats Plus Syndrome: A Patient Presenting with Extreme Short Stature as a Hallmark Feature

      hrp0092p1-228
    • "Endocrine Evaluation of 29 Cornelia de Lange Syndrome Patients (CdLS) Patients"

      hrp0092p1-229
    • Prognostic Factors of the Growth Hormone Therapy Effectiveness in Children with Turner Syndrome

      hrp0092p1-230
    • Height and Weight Dynamics in Preschool Boys with Constitutional Delay of Growth and Puberty

      hrp0092p1-231
    • Two Chinese Children with FBN1-Related Acromelic Dysplasia

      hrp0092p1-232
    • Growth Patterns Over Two Years After Birth According to the Birth Weight and Length Percentile in Children Born Preterm

      hrp0092p1-233
    • Identification of Syndromal Macrosomia: Macrocephaly, but Neither Height Nor Weight Data are Useful in the Detection of Pediatric PTEN Hamartoma Tumor Syndrome (PHTS)

      hrp0092p1-234
    • Development of a Measure for the Impacts of Achondroplasia on Children's Daily Functioning and Well-Being

      hrp0092p1-235
  • Multisystem Endocrine Disorders
  • • Serum Endocan Levels as a Marker of Endothelial Dysfunction in Turner Syndrome and Correlation with Cardiac Findings

      hrp0092p1-236
    • The Effects of Fetal Electromagnetic Field Exposure on Expression of Anxiety Behavior and Associated Genes in Adolescent Period

      hrp0092p1-237
    • Positive Correlation Between Circulating Irisin Concentrations and Homeostatic Model Assessment for Insulin Resistance (HOMA-IR) in Women with Polycystic Ovary Syndrome: A Meta-analysis

      hrp0092p1-238
    • Unusual Presentation of Autoimmune Polyglandular Syndrome Type 1 (aps1)

      hrp0092p1-239
    • Association of Tuberous Sclerosis Complex (TSC) and Insulinoma in a Pediatric Patient

      hrp0092p1-240
    • A Novel DCAF17 Homozygous Mutation in a Girl with Woodhouse-Sakati Syndrome and its Role in the Endocrine Glands

      hrp0092p1-241
    • Basal Metabolic Rate in Polycystic Ovary Syndrome: A Meta-Analysis

      hrp0092p1-242
    • A Nation-Wide Questionnaire Survey Targeting Japanese Pediatric Endocrinologists Regarding Transitional Care in Pediatric and Adolescent Cancer Patients

      hrp0092p1-243
    • Two Different Endocrine Cancer, One Disease; DICER-1 Mutation

      hrp0092p1-244
    • PTEN Hamartoma Tumor Syndrome (Overlap of Cowden syndrome and the Bannayan-Riley-Ruvalcaba Syndrome): Case Report

      hrp0092p1-245
    • Knowledge of the Natural History of Paediatric MEN1 is Required to Inform Decision Making for Predictive Testing in Childhood

      hrp0092p1-246
    • One AIRE Gene Mutation and Two Different Clinical Manifestations in a Couple of Brothers

      hrp0092p1-247
    • A Novel AIRE Gene Mutation in Two Siblings Revealing Different Phenotypes of Autoimmune Polyendocrine Syndrome Type 1

      hrp0092p1-248
  • Pituitary, Neuroendocrinology and Puberty (1)
  • • Use of Desmopressin for Bilateral Inferior Petrosal Sinus Sampling (BIPSS) in Pediatric Patients with Cushing Disease (CD)

      hrp0092p1-249
    • Correlation Between Pubertal Growth and Testicular Volume in Boys –a Longitudinal Study

      hrp0092p1-250
    • Central Diabetes Insipidus in Children: Role of GH Antibodies

      hrp0092p1-251
    • Brain Malformations and Sellar Spine as Possible Causes of Central Precocious Puberty in a Large Monocentric Study

      hrp0092p1-252
    • Changes in the Body Mass Index in Children with Central Precocious Puberty' Under Gonadotropin-Releasing Hormone Analogue Treatment - A Multicentric Study

      hrp0092p1-253
    • A Novel Approach for the Evaluation of Hypothalamic-Pituitary Region in Patients with Growth Hormone Deficiency: Pons Ratio

      hrp0092p1-254
    • Effects of 5-Hydroxymethylfurfural on Pubertal Development of Wistar Rats

      hrp0092p1-255
    • Kisspeptin Levels is a New Diagnostic Approach of Hypogonadotropic Hypogonadism in Boys

      hrp0092p1-256
    • Fetal and Post-Natal Growth are Impaired in Children with Deletions of the GH1 Gene: Description of a Cohort of 14 Patients

      hrp0092p1-257
    • Novel Pubertal References for Girls Using Ultrasound to Stage Breast Development. The Bergen Growth Study 2

      hrp0092p1-258
    • Disruption of Hypothalamic Regulation of Appetite Associated with Proton Beam Therapy

      hrp0092p1-259
    • A Case-Control Study of Exposure to Bisphenol-A and Phthalates in Girls with Early Onset of Puberty

      hrp0092p1-260
  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology (1)
  • • Long-Term Urological and Psychosexual Outcome of Men Born with Hypospadias

      hrp0092p1-261
    • Long-Term Outcome in Leydig Cell Hypoplasia

      hrp0092p1-262
    • Clinical and Molecular Characteristics, Genotype-Phenotype Correlation in 113 Chinese Children with SRD5A2 Gene Mutations

      hrp0092p1-263
    • Regulation of CBX2 Transcription in Human Development

      hrp0092p1-264
    • Dynamics in Blood Pressure After Pubertal Suppression with GnRH Analogs Followed by Testosterone Treatment in Male Adolescents

      hrp0092p1-265
    • A Nationwide Study of the Prevalence & Initial Management of Atypical Genitalia & Delayed Sex Assignment in the Newborn

      hrp0092p1-266
    • Endocrine Profiling and Association with Ultrasound Measured Testicular Volume and Biometrics in a Cohort of Norwegian Boys

      hrp0092p1-267
    • Idiopathic Scoliosis in Girls with Central Precocious Puberty: Incidence and Effect of Gonadotropin-Releasing Hormone Agonists

      hrp0092p1-268
    • The Impact of Klinefelter Syndrome on Quality of Life – a Multicentre Study

      hrp0092p1-269
    • Large Spectrum of DSD Phenotype Caused by Pathogenic Variants in Wilms Tumor Suppressor Gene 1

      hrp0092p1-270
    • Endocrine and Reproductive Outcome of Men Born with Various Degrees of Hypospadias

      hrp0092p1-271
    • Age at Menarche Over the Last Decades and Inter-Regional Variability in Northern Spain

      hrp0092p1-272
    • Hypergonadotropic Hypogonadism in 46, XX Adolescents Without Gonadotoxic Therapy: Clinical Features and Molecular Etiologies

      hrp0092p1-273
    • Quality of Life in Chilean Transgender Children, Adolescents, and Their Parents

      hrp0092p1-274
    • Long-Term Outcome of Testicular Function in Nonclassic Lipoid Congenital Adrenal Hyperplasia

      hrp0092p1-275
    • A Cross Sectional Study of Serum Gonadotropins, Testosterone and Genital Parameters During Mini Puberty in Normal Male Infants

      hrp0092p1-276
    • New Insights from Unbiased Panel and Whole-Exome Sequencing in a Large Chinese Cohort with Disorders of Sex Development

      hrp0092p1-277
    • A Novel MAP3K1 Gene Mutation (c.556A>G) Associated with 46, XY Complete Gonadal Dysgenesis

      hrp0092p1-278
    • Gender Mender, or Defender: Understanding Decision Making in Aotearoa/New Zealand for People Born with a Variation in Sex Characteristics

      hrp0092p1-279
    • Glucose Tolerance and Beta Cell Function in Adolescents with Polycystic Ovary Syndrome From North India

      hrp0092p1-280
    • Virilization of a Girl at Puberty Due to a Unique Translocation of an Abnormal Duplicated Y-Chromosome to a Deleted Chromosome 9 Including the DMRT1 Gene

      hrp0092p1-281
    • Characteristics of 311 Children with Early Onset Pubertal Signs. Descriptive Study

      hrp0092p1-282
  • Thyroid (1)
  • • Children with Hashimoto's Thyroiditis have Increased Intestinal Permeability: Results of a Pilot Study

      hrp0092p1-283
    • Different Endocrine Affects in DICER-1 Syndrome

      hrp0092p1-284
    • Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases

      hrp0092p1-285
    • Identification of a THRA Mutation in a 2yr Old Child with Clinical Features of Hypothyroidism and Multisystem Involvement

      hrp0092p1-286
    • The Comparison of Natural Course Thyroid Autoimmunity in Children and Adults with Type 1 Diabetes: From the Diabetes Onset Up to Five Years of its Duration

      hrp0092p1-287
    • Outcomes of Persistent Hyperthyrotropinaemia in Well Term Infants

      hrp0092p1-288
    • Thyroid Peroxidase Antibodies in Children with HLA-Conferred Susceptibility to Type 1 Diabetes

      hrp0092p1-289
    • Prediction of Permanent and Transient Congenital Hypothyroidism Based on Levothyroxine Dosages in Long-Term Follow-Up Patients: A Multicenter Retrospective Study in Japan

      hrp0092p1-290
    • An Incidental Finding of Thyroid Hormone Resistance Due to a De Novo Mutation in the THRB Gene

      hrp0092p1-291
    • Outcome of Congenital Hypothyroidism in Algeria: The Urgent Need to Implement a National Newborn Screening Program

      hrp0092p1-292
    • Genetic Susceptibility to Hashimito's Thyroiditis in Children: Analysis of Polymorphisms rs7093069 – IL2RA, rs5742909 – CTLA 4, rs7138803 – FAIM2

      hrp0092p1-293
    • Effect of serum TSH level on ovarian volume in prepubertal girls with subclinical hypothyroidism

      hrp0092p1-294
    • The Natural History of Delayed TSH Elevation in Neonatal Intensive Care (NICU) Newborns

      hrp0092p1-295
  • Adrenals and HPA Axis (2)
  • • Three Novel Mutations of the StAR Gene in Five Algerian Patients Presenting with Classical and Non-Classical Lipoid Adrenal Hyperplasia

      hrp0092p1-296
    • A Novel Compound Heterozygous Mutation in the CYP11B2 Gene, Including an Intron 7 Splice Site, is Responsible for Aldosterone Synthase Deficiency Type II

      hrp0092p1-297
    • First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly Each Other with in 21-Hydroxylase Deficiency

      hrp0092p1-298
    • Medical Identification Jewellery Use in Children and Young Adults with Adrenal Insufficiency

      hrp0092p1-299
    • Growth Trajectory and Final Height in Children with Non Classical Congenital Adrenal Hyperplasia

      hrp0092p1-300
    • Height in Infants Aged 1 Year with Classic Congenital Adrenal Hyperplasia is Related to their Urinary Steroid Metabolome

      hrp0092p1-301
    • MIRAGE Syndrome, a Novel Syndromic form of Primary Adrenal Insufficiency

      hrp0092p1-302
    • Hypothalamo-Pituitary-Adrenal (HPA) Axis in Infants Exposed to Corticosteroids During Fetal Life

      hrp0092p1-303
    • Identification of Novel and Rare CYP21A2 Variants in Chinese Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

      hrp0092p1-304
    • Clinical Manifestations & Molecular Analysis of Four Palestinian Patients with Pseudohypoaldosteronism Type 1 (PHA 1) Revealing Four Novel Mutations in the ENaC Subunit Genes

      hrp0092p1-305
    • Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience

      hrp0092p1-306
    • "CAH-X" Due to Homozygous Deletions of CYP21A2 and TNXB Exon 35 in a Newborn from the 17 OHP Screening

      hrp0092p1-307
  • Diabetes and Insulin (2)
  • • ABCC8 MODY in an Obese Adolescent Misdiagnosed with Type 2 Diabetes

      hrp0092p1-308
    • Level of Glycemic Control in Pediatric Patients with Type 1 Diabetes in Bern: A Cross-Sectional Study

      hrp0092p1-309
    • Preliminary Results of Public Health Prevention Program for Diabetic Ketoacidosis in Children and Adolescent

      hrp0092p1-310
    • Optimisation of Transfection Methods Using DNA, RNA and Protein Formats for CRISPR Cas9 Mediated Gene Knock out in Beta-TC-6 Cells.

      hrp0092p1-311
    • Treatment of Diabetic Ketoacidosis with Sub-Cutaneous Regular Insulin in Non-ICU Setting is Economical and Results in Rapid Recovery

      hrp0092p1-312
    • Familial Versus Non-Familial Type-2 Diabetes Mellitus in Children and Adolescents: Clinical and Biochemical Data.

      hrp0092p1-313
    • Comparison Between Patients and Families who Routinely Download Data and Those who do Not Download Data at Home in The Management of Type 1 Diabetes

      hrp0092p1-314
    • Immune Status in Children and Adolescents with Type 1 Diabetes

      hrp0092p1-315
    • An Evaluation of the Accuracy of a Flash Glucose Monitoring System in Children with Diabetes in Comparison with Venous Blood Glucose

      hrp0092p1-316
    • Unexplained Neonatal Deaths Among Kurdish Consanguineous Families: Importance of Recognizing Congenital Hyperinsulinism and Testing for KATP Channel Gene Variants

      hrp0092p1-317
    • Improving The Transition to Adult Care for Adolescents with Type 1 Diabetes: Effect of Transition Readiness, Self-Efficacy and Diabetes Distress on Glycemic Control During Transition

      hrp0092p1-318
    • Gene Dosage Changes in the GCK Gene not Detected by Sanger DNA Sequencing in Two Patients with Phenotypic MODY 2

      hrp0092p1-319
    • Assessment of Vascular Endothelial Dysfunction Using Brachial Artery Flow Mediated Dilatation and Carotid Intima Media Thickness in Children and Adolescents with Type 1 Diabetes

      hrp0092p1-320
    • A Case of Late-Onset Monogenic Diabetes Due to a Homozygous Variant in the GCK Gene

      hrp0092p1-321
    • Neonatal Diabetes and Glis3 Mutation: A New Phenotype

      hrp0092p1-322
    • Diabetes Type 2 in Non-Obese Neurologically Impaired Children and Adolescents: A New Emerging Entity?

      hrp0092p1-323
    • Cataract in Type 1 Diabetes Mellitus Patients- a Nationwide Population-Based Study

      hrp0092p1-324
    • Association of CTLA-4 Gene with the Familial Diabetes Mellitus

      hrp0092p1-325
    • Copy Number Variation (CNV) Sequencing Identifies a Novel Mutation of the Glucokinase Gene in Maturity-Onset Diabetes of the Young

      hrp0092p1-326
    • The Paediatric Diabetes Service in England and Wales – Learning from Sweden's Improvement Journey.

      hrp0092p1-327
    • Creating a Neural Network Model Based on Glycemic Variability Indices to Predict the Degree of Compensation for Type 1 Diabetes

      hrp0092p1-328
    • Evaluation of AGP Reports in Patients with Type 1 Diabetes Using Intermittently Viewed Continuous Glucose Measurement System (iCGM)

      hrp0092p1-329
    • Evaluation of Clinical, Laboratory and Therapeutic Features and Long Term Follow-up Results in 44 Cases with Genetic Diagnosis of MODY; Single Center Experience

      hrp0092p1-330
    • Design and Implementation of an Integral System of Clinical Follow-Up and Glucose Monitoring in Children Affected of Type 1 Diabetes, in Andalusia

      hrp0092p1-331
    • Targeted Next-Generation Sequencing Demonstrates High Frequency of MODY in Russian Children.

      hrp0092p1-332
    • Abdominal Fat Distribution Assessed by Abdominal CT Scan in Adolescents with Type 2 Diabetes Mellitus

      hrp0092p1-333
  • Fat, Metabolism and Obesity (2)
  • • ADCY3 Genetic Variants in Cypriot Obese Children

      hrp0092p1-334
    • The Relationship Between Serum Neurotensin Levels and Metabolic Parameters and Eating Behavior in Obese Children

      hrp0092p1-335
    • Genomic Knowledge as the Powerful Tool to Understand the Obesity

      hrp0092p1-336
    • How does Clusters of Parental Characteristics Influences Offspring Adiposity: A Prospective Study

      hrp0092p1-337
    • Continuous Score of Metabolic Syndrome (sSMp) in Chilean Pediatric Population is Associated with Insulin Resistance Parameters and Subclinical Endothelial Inflammation

      hrp0092p1-338
    • Elevated High-Sensitivity C-Reactive Protein Level is Associated with Prediabetes and Adiposity in Korean Children and Adolescents.

      hrp0092p1-339
    • Secular Change in Waist Circumference and Waist-Height Ratio in Korean Children and Adolescents Over 10 Years and Effort to Identity Optimal Cutoff for Cardiometabolic Risk

      hrp0092p1-340
    • ANGPTL2 and ANGPTL3 in Children with Obesity and Metabolic Syndrome

      hrp0092p1-341
    • Can Increased First Hour Glucose Concentration in OGTT Be a New Indicator in Projecting Metabolic Profile?

      hrp0092p1-342
    • Perinatal Features of Prader-Willi Syndrome: A Chinese Cohort

      hrp0092p1-343
    • The Adipokine Leptin is Associated with Adiposity in Survivors of Childhood Brain Tumours: A Preliminary Report from the Canadian Study of Determinants of Endometabolic Health in Children (CanDECIDE Study)

      hrp0092p1-344
    • ANGPTL-4 in Children and Adolescents: Relation to Gender, Puberty and Obesity

      hrp0092p1-345
    • Non-Invasive Assessment of Liver Steatosis: Usefulness of Elastography in Obese Children – a Pilot Study.

      hrp0092p1-346
    • Precocious Pubarche in Spinal Muscular Atrophy Patients with Severe Sarcopenia

      hrp0092p1-347
    • Evaluation of the Relationship Between Serum Uric Acid Level and Cardiometabolic Risk in Obese Children and Adolescents

      hrp0092p1-348
    • Prevalence of Dyslipidemia in Korean Youth Over 10 Years: Data from the Korea National Health and Nutrition Examination Survey 2008-2017

      hrp0092p1-349
    • Metabolic Risk in Long-Term Survivors of Childhood Acute Lymphoblastic Leukemia

      hrp0092p1-350
    • Congenital Generalized Lipodystrophy Type 4 - New Mutation in the CAVIN1 Gene

      hrp0092p1-351
    • Paediatric Patients with Type 1 Diabetes Mellitus Exhibit Reduced Brown Adipose Tissue Heat Signature Following Cold Stimulation

      hrp0092p1-352
    • Evaluation of Primary Hypertriglyceridemia Patients: Ethiology, Phenotype, Treatment

      hrp0092p1-353
    • Association Between Adiposity Measures and Metabolic Variables in Children and Adolescentswith Obesity

      hrp0092p1-354
    • A Comparison of Insulin Resistance Indices: HOMA and Belfiore in 6-8-Year-Old, Properly Growing Children, Born Small for Gestational Age

      hrp0092p1-355
    • The «Double Diabetes» in Adolescent with Prader-Willi Syndrome.

      hrp0092p1-356
    • Evaluation of Body Composition and Resting Metabolic Rate in Adolescents with KS

      hrp0092p1-357
    • Relationship Between RBP4 Level and Two of its Gene Polymorphisms with Body Composition and Metabolic Profile in Obese Children

      hrp0092p1-358
  • GH and IGFs (2)
  • • Insulin-Like Growth Factor 2 in Pediatric Gliomas: Expression, Intracellular Localization and Association with Clinical Outcome

      hrp0092p1-359
    • Prevalence of Children Born Small for Gestational Age with Short Stature who Qualify for Growth Hormone Treatment: A Preliminary Population-Based Study

      hrp0092p1-360
    • Long-Term Safety of a Once-Weekly Somatrogon (hGH-CTP): 4-Year Results of a Phase 2 Extension Study in Children with Growth Hormone Deficiency

      hrp0092p1-361
    • Sequencing Approach to Identify Candidate Genes Involved in Short Stature

      hrp0092p1-362
    • Metabolism of Somapacitan, a Long-Acting Growth Hormone Derivative, in Human Subjects

      hrp0092p1-363
    • GH Values in Serum and Blood Spots on Filter Paper Samples in Neonates Until 30 Days of Life by Electrochemiluminescence (ECLIA).

      hrp0092p1-364
    • De Novo Formation of Neutralizing IGF-I Antibodies During rhIGF-1 Treatment in a Girl with IGFALS Deficiency as Distinct Adverse Event Interfering with Growth Promotion

      hrp0092p1-365
    • Glomerular Filtration Rate in Young Adults Born SGA: A 5-Year Longitudinal Study after Cessation of GH Treatment.

      hrp0092p1-366
    • Normal IGF-Bioactivity and Low Free IGF-I in Patients with Prader-Willi Syndrome with High Total Serum IGF-I: Immunoreactive IGF-I Concentration Poorly Reflects IGF Bio-Activity and Bio-Availability.

      hrp0092p1-367
    • Renal Complication of Hematuria and Proteinuria after Recombinant Human Growth Hormone Therapy in Children

      hrp0092p1-368
    • Detection and Referral of Children with Short Stature in Serbia - the Impact of Electronic Growth Charts

      hrp0092p1-369
    • Challenges Experienced in Delivering Growth Hormone Therapy in Children's with Prader Willi Syndrome in Birmingham Children's Hospital.

      hrp0092p1-370
  • Growth and Syndromes (to include Turner Syndrome) (2)
  • • Growth Hormone Deficiency (GHD): Assessing Parent Burden for Child Growth Hormone Deficiency Treatment: The Growth Hormone Deficiency - Parent Treatment Burden Measure (GHD-PTB)

      hrp0092p1-371
    • A Considerable Role of NPR2 Mutation in Idiopathic Short Stature: Identification of Two Novel Mutations

      hrp0092p1-372
    • Matrix Metalloproteinases, their Inhibitors and Neurotrophic Factors as Indicators of Cardiometabolic Risk in Turner Syndrome Girls

      hrp0092p1-373
    • Growth in the First Ten Years after Antiretroviral Therapy Initiation Among HIV-Infected Children in the CoRISpe Spanish Pediatric Cohort.

      hrp0092p1-374
    • SOAR Study: New Approaches to Managing Social Skills Deficits in Turner Syndrome

      hrp0092p1-375
    • Noonan Syndrome (NS) Spectrum Panels should Include Mutations in LZTR1 Gene

      hrp0092p1-376
    • International Consensus: Ovarian Tissue Cryopreservation in Young Turner Syndrome Patients. Outcomes of an Ethical Delphi Study Including 55 Experts from 16 Different Countries.

      hrp0092p1-377
    • Vascular Anomalies and Aortic Dilatation in Turner Syndrome Study in a Large Cohort of Young-Adult Patients

      hrp0092p1-378
    • Adult Height Prediction by Bone Age Determination in Children with Idiopathic Growth Hormone Deficiency (IGHD): Analysis of KIGS Data

      hrp0092p1-379
    • A New Model of Adult Height Prediction Validated in Boys with Constitutional Delay of Growth and Puberty

      hrp0092p1-380
    • The Relation Between Changes in Body Mass Index (BMI) and Linear Growth in Prepubertal Children: Daily Weight Gain and BMI Changes in Relation to Linear Growth During Nutritional Rehabilitation of Underweight Children.

      hrp0092p1-381
    • Nutritional Requirements in Prader Willi Syndrome Children Treated with Growth Hormone Under Two Years of Age

      hrp0092p1-382
    • Cardiovascular Anomalies and Association with Karyotypes in Turner Syndrome in Taiwan: One Medical Center Experience

      hrp0092p1-383
    • Pubertal Induction Amongst Girls with Turner Syndrome: A Review of Changing Practice Over 10 Years.

      hrp0092p1-384
    • Saliva Might be a Good Alternative DNA Source for Whole Exome Sequencing to Identify Genetic Causes of Short Stature

      hrp0092p1-385
    • Prevalence of Copy Number Variations (CNVs) in a Cohort of SGA Children with Persistent short Stature Associated with Additional Clinical Features.

      hrp0092p1-386
    • Omnitrope® (Recombinant Human Growth Hormone) in Short Children Born Small for Gestational Age (SGA): A Long-Term, Phase IV Study

      hrp0092p1-387
    • Is there a QTc Interval Prolongation in Girls and Women with Turner Syndrome?

      hrp0092p1-388
    • Eight Years of Growth Hormone Treatment in a Patient with Schaaf-Yang Syndrome

      hrp0092p1-389
    • Genetic Evaluation of Idiopathic Short Stature

      hrp0092p1-390
    • Foramen Magnum Stenosis (FMS): Neuroradiological Aspects before and after Cervical Decompression in Paediatric Patients with Achondroplasia (ACH).The 'Achondroplasia Multidisciplinary Gaslini's Group' (AMGG) Istituto Giannina Gaslini, Genova, Italy: Child Neuropsychiatry Unit, Neuroradiology Unit, Department of Paediatrics, Neurosurgery Unit, Orthopedic Unit, Rehabilitation Unit, Pulmonary Disease and Allergy Unit.

      hrp0092p1-391
    • Do Children and Adolescents with Idiopathic short Stature show Postural Alterations? Possible Influence of SHOX Haploinsufficiency in a Pilot Study

      hrp0092p1-392
    • Evaluation of Body Composition and Resting Metabolic Rate in Children with Growth Hormone Deficiency

      hrp0092p1-393
  • Pituitary, Neuroendocrinology and Puberty (2)
  • • Next Generation Sequencing in GnRH Deficient Patients with Congenital Hypogonadotrophic Hypogonadism: Novel Findings in KAL1, SRA1, WDR11, FGFR1, CHD7 and PROP1 Genes

      hrp0092p1-394
    • Presentation and Diagnosis of Childhood Onset Combined Pituitary Hormone Deficiency: A Single Center Experience from Over 30 Years.

      hrp0092p1-395
    • The Relationship Between Precocious Puberty and Premature Thelarche withSerum Irisin Levels

      hrp0092p1-396
    • Questioning the Value of Brain MRIs in the Evaluation of Children with Isolated Growth Hormone Deficiency

      hrp0092p1-397
    • Postoperative Quality of Life in Children and Adolescents with Craniopharyngioma – Results of the Prospective Multicenter Trial KRANIOPHARYNGEOM 2007

      hrp0092p1-398
    • Pubertal Events, Reproductive and Growth Hormones and Predictive Factors in Healthy Girls with Transient Thelarche.

      hrp0092p1-399
    • Plasma Copeptin Distribution in the Pediatric Age: A Useful Diagnostic Tool for AVP-Related Disorders

      hrp0092p1-400
    • Management and Treatment Outcome of Childhood-Onset Craniopharyngioma (CP) in Italy: Multicentre Collection of 117 Cases

      hrp0092p1-401
    • Evaluation of Brain Mri Lesions in 381 Girls with Central Precocious Puberty

      hrp0092p1-402
    • Xanthomatous Hypophysitis: A Rare Case in a Paediatric Patient

      hrp0092p1-403
    • Improvement of Final Height in Idiopathic Central Precocious Puberty is Associated with Delay of Bone Maturation with GnRH Agonist Therapy Under the Age of 7 Years

      hrp0092p1-404
    • Metabolic Changes in Children Treated for Medulloblastoma

      hrp0092p1-405
    • Tolvaptan for Management of Intractable Salt and Water Imbalance in a Case with Suprasellar Tumor after Surgery

      hrp0092p1-406
    • No Association Between Serum Level of NPTX 1 and MKRN3 in Central Precocious Puberty

      hrp0092p1-407
    • Training in Pubertal Assessment – First Step to the Observational Pilot Study PROSPEL (Premier Observatoire des Stades Pubertaires en Libéral)

      hrp0092p1-408
  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology (2)
  • • Long-Term Outcome in Young Women Treated for Central Precocious Puberty

      hrp0092p1-409
    • Sertoli Cell Function after Chemotherapy in Boys with Hematologic Malignancies

      hrp0092p1-410
    • Gender Decision in Disorders of Sex Development (DSD) Patients: 20 Years' Experience

      hrp0092p1-411
    • WES Analysis of a Cohort of 94 Patients Presenting with 46,XY and 46,XX DSD

      hrp0092p1-412
    • Assessment of the Function of Lower Urinary Tract Following Feminizing Genitoplasty in Females with Congenital Adrenal Hyperplasia

      hrp0092p1-413
    • Gonadal Insufficiency and Affecting Factors in Patients with Bone MarrowTransplantation(BMT) for Non-malignantIndications in Childhood or Adolescence

      hrp0092p1-414
    • Clinical and Molecular Characteristics of Russian Patients with 46,XY DSD due to NR5A1 Gene Mutations.

      hrp0092p1-415
    • Creating a Clinical Evaluation System for Simple and Comprehensive Scoring of Differences/Disorders of Sexual Development

      hrp0092p1-416
    • Hypospadias: Clinical Approach, Surgical Technique and Outcome. Twenty Years' Experience of a Single Centre.

      hrp0092p1-417
    • Epidemiology of Diagnoses of Sex Development Disorders Based on the Registry of Rare Diseases, in a Large Area of North-Eastern Italy

      hrp0092p1-418
    • Premature Ovarian Insufficiency in Women after Treatment for Childhoodcancer is a Risk Factor for Metabolic Syndrome

      hrp0092p1-419
  • Thyroid (2)
  • • The Genetic and Clinical Characteristic of Pediatric Patients with Congenital Hypothyroidism Gland In-Situ

      hrp0092p1-420
    • Zinc Transporter 8 (ZnT8) as a New Autoantigen in Thyroid Tissue – Preliminary Data

      hrp0092p1-421
    • Prospective Evaluation of Autoimmune and Non-Autoimmune Subclinical Hypothyroidism in a Large Cohort of Children and Adolescents with Down Syndrome

      hrp0092p1-422
    • Congenital Hypothyroidism (CH) Detected by the Second Newborn Screening in Lombardia Region: Incidence and Evolution of CH

      hrp0092p1-423
    • Transition for Patients with Chronic Thyroid Diseases

      hrp0092p1-424
    • Maternally Inherited Resistance to Thyroid Hormones with Discordant Postnatal Phenotypes in Two Infant Brothers

      hrp0092p1-425
    • A Rare Case of Familial Heterozygous Thyroid Hormone Receptor Beta (THRB) Mutation Presenting with Dilated Cardiomyopathy

      hrp0092p1-426
    • Acquired Hypothyroidism in a Toddler: An Unusual Presentation of Langerhans Cell Histiocytosis

      hrp0092p1-427
    • Anti-Gastric Parietal Cells Antibodies for Autoimmune Gastritis Screening: A Follow-Up Study in Young Patients with Autoimmune Thyroid Disease.

      hrp0092p1-428
    • Genetic Evaluation of Congenital Hypothyroidism with Gland-In-Situ Using Targeted Exome Sequencing

      hrp0092p1-429
    • Clinical Characteristics and Long-Term Follow-Up of Patients with Congenital Hypothyroidism (CH) due to Thyroid Peroxidase (TPO) Gene Mutations

      hrp0092p1-430
    • The Relationship Between Perfluoroalkyl Compounds Concentrations at Ages 2, 4, and 6 Years and Thyroid Function in Early Childhood: A Prospective Cohort Study

      hrp0092p1-431
    • Levothyroxine Effect on Thyroid Volume in Children with Autoimmune Hashimoto Thyroiditis (AHT) Presenting Subclinical (SH) or Overt (Oh) Hypothyroidism

      hrp0092p1-432
  • Late Breaking Posters
  • • A Trial Investigating the Long-Term Efficacy and Safety of Two Doses of Norditropin® (Somatropin; Recombinant Human Growth Hormone) in Japanese Children with Short Stature Due to Noonan Syndrome Over Four Years of Treatment

      hrp0092lb-1
    • The Effects of Different Diets (High Fat and High Fructose Diet) on the Development of Insulin Resistance and Tissue Advanced Glycation End Product Levels in Rats

      hrp0092lb-2
    • Insights into the Regulation of Androgen Biosynthesis from Males with Congenital Hypogonadotropic Hypogonadism: Quantification of Bioactive Steroid Hormones Reveals Differences Between Gonadotropin Replacement and Testosterone Replacement

      hrp0092lb-3
    • Resistance to Thyroid Hormone Alpha Associated with Early-Onset Severe NASH

      hrp0092lb-4
    • Height Curves and Height SDS in ADHD Children Measured Before and After Stimulant Treatment are not Affected - Observation Study in 7172 ADHD Children

      hrp0092lb-5
    • Can Different Diets (High Fat and High Fructose Diet) Affect Insulin Resistance, Tissue Advanced Glycation End Product Levels in Rats' Pancreas

      hrp0092lb-6
    • Long-Term Evaluation of Ovarian Function and Follicular Reserve in Patients with Malignant Diseases Treated with Chemotherapy in Prepubertal or Pubertal Age

      hrp0092lb-7
    • Detection of Cardiomyopathy in Egyptian Children and Adolescents with Longstanding Obesity Using Cardiac Marker NT-pro PNB and Speckled Tracking Echocardiography

      hrp0092lb-8
    • Left Ventricular Mass Index and Cardiovascular Function in Adolescents Born Small for Gestational Age (SGA)

      hrp0092lb-9
    • Irisin as a Mediator between Obesity and Vascular Inflammation in Chinese Children and Adolescents

      hrp0092lb-10
    • Height in Inborn Errors of Metabolism Requiring Hypoprotidic Diet: A Longitudinal Follow Up Study About 213 Patients

      hrp0092lb-11
    • Thyroid Function in Neonates Conceived After Hysterosalpingography with Iodinated Contrast Media

      hrp0092lb-12
    • Gut Hormones Secretion Across Clusters of Metabolic Syndrome in Obese Prepubertal Children

      hrp0092lb-13
    • Prenatal Smoke-Exposure is Associated with Increased Anogenital Distance in Female Infants

      hrp0092lb-14
    • Efficacy of 3-Monthly Compare to Monthly Depot GnRH Agonist (Triptorelin Pamoate) in the Treatment of Girls with Central Precocious Puberty in Korea

      hrp0092lb-15
    • Associations Between Pituitary Abnormalities and Treatment Response in Children with Growth Hormone Deficiency. First Multicenter Study in Portugal

      hrp0092lb-16
    • Assessment of Urinary Podocalyxin as a Marker of Glomerular Injury in Obesity Related Kidney Disease in Obese Children and Adolescents compared to urinary Albumin-creatinine ratio

      hrp0092lb-17
    • Exploratory Case-Control Study on ACE2 Expression in Children with Short Stature

      hrp0092lb-18
    • CDX2 Polymorphism of VDR Gene and Lipid Profile in Patients Treated for Acute Lymphoblastic Leukemia During Childhood

      hrp0092lb-19
    • IIntroduction of Flash Glucose Monitoring in Children with Type 1 Diabetes: Experience of a Single-Centre in Spain

      hrp0092lb-20
    • How Can the Occurrence of Delayed Elevation of Thyroid Stimulating Hormone in Preterm Infants Born Between 35 and 36 Weeks Gestation be Predicted?

      hrp0092lb-21
    • Two Novel Mutations of The LHX3 Gene Associated with a Severe Phenotype Involving Endocrine, Nervous and Skeletal Systems

      hrp0092lb-22
    • Long-Term Safety and Effectiveness of Recombinant Human Growth Hormone in Korean Pediatric Patients with Growth Disorders: 7-year Interim Analysis from LG Growth Study

      hrp0092lb-23
    • Abdominal Adiposity and Total Body Fat as Predictors of Cardiometabolic Health in Pre-Pubertal and Pubertal Youth

      hrp0092lb-24
    • Low Trabecular Bone Score in Children with Inflammatory Bowel Diseases

      hrp0092lb-25
    • Dramatic Clinical Response to Lenvatinib in One Pediatric Patient with Advanced Metastatic Papillary Thyroid Carcinoma

      hrp0092lb-26
    • Does Karyotyping and in situ Hybridization from Three Different Germ Layers Elucidate Low Bone Mineral Density in Turner Syndrome?

      hrp0092lb-27
    • The Volumetric Changes in the Olfactory Bulb Depend on Body Mass Index

      hrp0092lb-28
• Poster Category 2
• • Adrenals and HPA Axis
  • • Gender Identity, Sexual Orientation and Quality of Life in Women with Non-classic Congenital Adrenal Hyperplasia

      hrp0092p2-1
    • CYP11A1 (Side-chain Cleavage Enzyme) Defect in Three Brothers Causing Glucocorticoid and Mineralocorticoid Deficiency and Development of Testicular Adrenal Rest Testicular Tumour

      hrp0092p2-2
    • Contraceptives in Female Adolescents with 21-hydroxylase Deficiency (CAH) - a way to Optimize Treatment with Respect to Androgen Excess? A Pilot Study

      hrp0092p2-3
    • Bone Age Advancement in Prepubertal Children with Premature Adrenarche

      hrp0092p2-4
    • Clinical Phenotype and Genotype Association in Patients with 21-hydroxylase Deficiency

      hrp0092p2-5
    • Corticosteroid Use: Practices and Attitudes of Pediatricians

      hrp0092p2-6
    • Updates on Genotype and Phenotype of Vietnamese Patients with X-Linked Adrenoleukodystrophy

      hrp0092p2-7
    • Novel TBX19 Mutation as Cause of Hypoglicemia in Two Siblings

      hrp0092p2-8
    • The Clinical Polymorphism and Variability of X-linked Adrenoleukodystrophy in One Russian Family

      hrp0092p2-9
    • Functional Adrenocortical Oncocytoma – a Rare Cause of Progressive Virilization and Secondary Amenorrhea

      hrp0092p2-10
    • Long-term Prednisone versus Hydrocortisone Treatment in Children with Classic Congenital Adrenal Hyperplasia (CAH): A Controlled Study

      hrp0092p2-11
    • A Case of X-linked Adrenoleukodystrophy Presenting with Primary Adrenal Insufficiency and Normal VLCFA

      hrp0092p2-12
    • Different Potent Glucocorticoids, Different Routes of Exposure but The Same Result: Iatrogenic Cushing's syndrome and Adrenal Insufficiency

      hrp0092p2-13
    • Differences Between Normal-bmi Girls with Premature Adrenarche and Overweight or Obese Girls with Premature Adrenarche

      hrp0092p2-14
    • Rare Causes of Primary Adrenal Insufficiency at King Faisal Specialist Hospital Retrospective Study

      hrp0092p2-15
    • A Case of Infantile Cushing's Syndrome from McCune Albright Syndrome: The Importance of Multiple-Site Sampling for Genetic Testing

      hrp0092p2-16
    • Duodenal Web Presenting as Pseuhypoaldosteronism in Infancy

      hrp0092p2-17
    • A Rare Case of Pseudohypoaldosteronism in a Neonate Secondary to Congenital Hydrometrocolpos

      hrp0092p2-18
    • Hyperandrogenism in a 13-year-old Girl due to Glucocorticoid Receptor Mutation

      hrp0092p2-19
    • Polydipsia, Hyponatremia and a Biochemical Profile of Aldosterone Synthase Deficiency

      hrp0092p2-20
    • Fludrocortisone Treatment in a Child with Postural Orthostatic Tachycardia Syndrome (POTS): A Case Report

      hrp0092p2-21
    • An Atypical Case of Ectopic ACTH Syndrome in an Adolescent Boy

      hrp0092p2-22
    • "Girls with Idiopathic Premature Adrenarche Achieve Normal Adult Height"

      hrp0092p2-23
    • Adult Height and Growth Pattern in Patients with Classic Congenital Adrenal Hyperplasia

      hrp0092p2-24
    • Cushing Syndrome due to an Adrenacortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

      hrp0092p2-25
  • Bone, Growth Plate and Mineral Metabolism
  • • Successful Parathyroidectomy with Intraoperative Parathyroid Hormone Monitoring in a Neonate with Severe Primary Hyperparathyroidism due to a Novel CASR Mutation

      hrp0092p2-26
    • The First Case Report of SEMD-JL1 in China

      hrp0092p2-27
    • Clinical Radiographic and Biochemical Findings of Three Patients with Hypophosphatasia Carrying the Same Mutation

      hrp0092p2-28
    • Clinical and Genetic Characteristics of Pseudohypoparathyroidism Type 1A in Children Based on Single-center Cohort Study

      hrp0092p2-29
    • A Rare case of Neonatal Hypocalciuric Hypercalcemia Complicated with Arrhythmia

      hrp0092p2-30
    • Experience of Burosumab Therapy in Four Children with X-linked Hypophosphataemia in Saudi Arabia

      hrp0092p2-31
    • Pediatric Patients with Heterozygous ALPL Mutation show a Broad Clinical Phenotype

      hrp0092p2-32
    • Growth and Bone Mineral Density in Egyptian Children with Congenital Adrenal Hyperplasia on Glucocorticoid Replacement Therapy; A Single Center Study

      hrp0092p2-33
    • Chronic Bone Disease in Pediatric Sickle Cell Disease Including a Case of Successful Bisphosphonate Therapy

      hrp0092p2-34
    • Clinical and Genetic Characteristics of 168 Russian Patients with Hypophosphatemic Rickets

      hrp0092p2-35
    • A 10-year-old Girl with Primary Hypoparathyroidism and Systemic Lupus Erythematosus (SLE)

      hrp0092p2-36
    • An Unusual Case of Hyperparathyroidism: Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (FHHNC) Associated with Mutations in CLDN19

      hrp0092p2-37
    • Skeletal Maturity and Growth in children with Type 1 Diabetes

      hrp0092p2-38
    • Bone Mineral Status in Adults with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency

      hrp0092p2-39
    • Reduced Bone Mineral Density in Children with Inflammatory Bowel Disease without Exposure to Corticosteroid Treatment

      hrp0092p2-40
    • A Clinical Dilemma in the Detection of Paediatric Hypophosphataemia

      hrp0092p2-41
    • Stuve-Wiedemann Syndrome: A Case Report without Osteorosis

      hrp0092p2-42
    • A Rare Form of Vitamin D Receptors Dysfunction (vitamin D-dependent Rickets Type II) with Alopecia. A Case Report

      hrp0092p2-43
    • Cinacalcet Experience in Hypercalcemia Due to CaSR Mutation

      hrp0092p2-44
    • Two Siblings with Hypophosphatemic Rickets: SLC34A3 Gene Mutations with Different Clinical Phenotypes

      hrp0092p2-45
    • Seasonal 25-hydroxy Vitamin D3 Variations in School-aged Children from Santiago de Chile

      hrp0092p2-46
    • Vitamin D Deficiency among Children with Malignancy

      hrp0092p2-47
    • Novel Mutation of the Prkar1a Gene in a Girl with Clinical Diagnosis of Pseudohypoparathyroidism

      hrp0092p2-48
    • Successful Treatment with Enzyme Replacement Therapy in a Girl with Severe Infantile Hypophosphatasia

      hrp0092p2-49
    • Bone Mineral Density in Children with Type 1 Diabetes Mellitus (T1DM) and Analysis of Possible Factors Affecting Their Bone Health; A controlled study

      hrp0092p2-50
    • Perinatal form Hypophosphatasia Caused by a Novel Large Duplication of ALPL Gene and two year follow-up under Enzyme Replacement Therapy; A case report

      hrp0092p2-51
    • A rare cause of hypophosphatemia: Raine Syndrome

      hrp0092p2-52
    • Idiopathic Infantile Hypercalcemia: Mutations in SLC34A1 and CYP24A1 in Two Siblings and Fathers

      hrp0092p2-53
    • Crouzon Syndrome: A rare case report of a 2-month old boy with Micrognathia and Proptosis

      hrp0092p2-54
    • A Novel Missense COL10A1 Mutation Identified by Next Generation Sequencing in a Chinese Pedigree with Schmid Metaphyseal Chondrodysplasia

      hrp0092p2-55
    • a case report of a girl with short stature has laron syndrome and spondyloepimetaphyseal dysplasia

      hrp0092p2-56
    • A Novel Mutation of Phex Gene Inducing X-Linked Hypophosphatemia Rickets, A Case Report

      hrp0092p2-57
    • Skeleton Muscles and Tissues Metabolic Activity in Greek Adolescent PCOS

      hrp0092p2-58
    • Spondyloocular Syndrome: Presentation of Two Siblings Diagnosed with The Rare Disease and The Results of Pamidronate Therapy

      hrp0092p2-59
    • Clinical and Genetic Characterization of Tunisian Children with Hereditary Hypophosphatemic rickets (HHR).

      hrp0092p2-60
    • Osteogenesis Imperfecta: Genetic Evaluation

      hrp0092p2-61
  • Diabetes and Insulin
  • • The Effect of Carbohydrate Recognition and Counting Ability on Glycemic Control in Pediatric Patients with Type 1 Diabetes

      hrp0092p2-62
    • A Rare Case of Syndromic Diabetes due to an INSR Pathogenic Variant

      hrp0092p2-63
    • Autoimmune Thyroid Diseases in Children and Adolescents with Maturity Onset Diabetes of the Young

      hrp0092p2-64
    • Abstract unavailable

      hrp0092p2-65
    • New Mutation of the PDX-1 Gene Causes MODY Type 4 Diabetes in a 17 year old girl with Good Response to Oral Antidiabetics

      hrp0092p2-66
    • Periodontal Disease Among Children and Adolescents with Type 1 Diabetes Mellitus

      hrp0092p2-67
    • Pancreatic β Cell Function and its Relationship with Iron Overload in Patients with β-Thalassemia Major

      hrp0092p2-68
    • Gluten-free Diet in Children with Recent Onset Type 1 Diabetes is Associated with Slower Pace of C-peptide Decline, Better Metabolic Control and Lower Insulin Requirement at 12 months

      hrp0092p2-69
    • Evaluation of β-cell Function in Young MODY Patients using a Mixed Meal Tolerance Test

      hrp0092p2-70
    • The Effect of Different Forms of Maternal Dysglycemia on the occurrence of Neonatal Hypoglycemia in babies admitted to NICU.

      hrp0092p2-71
    • Adropin, Afamin And Neudesin - Novel Biomarkers of Type 1 Diabetes Mellitus in Children

      hrp0092p2-72
    • Prevalence, Time Trend and Predictors of Celiac Disease in Type 1 Diabetes

      hrp0092p2-73
    • Impact of the Flash Glucose Monitoring System on Children with Type 1 Diabetes After the First Year of Using in Systematic Way

      hrp0092p2-74
    • Insulin Treatment of Cystic Fibrosis Related Diabetes (CFRD) on BMI and Respiratory Function

      hrp0092p2-75
    • Coexistence of Medium chain acyl-CoA dehydrogenase deficiency (MCADD) and Type 1 diabetes (T1D): A management challenge

      hrp0092p2-76
    • Education in type 1 Diabetes Mellitus (T1D): what do Educators Really Know? A Tunisian Multicenter Study among Young Doctors, Nurses and Nutritionnists

      hrp0092p2-77
    • A Case of an Infant with Congenital Hyperinsulinism Complicated by Diabetic Ketoacidosis during Treatment

      hrp0092p2-78
    • Clinical Profile and Follow-up Analysis of Neonatal Diabetes Mellitus- Single Centre Experience

      hrp0092p2-79
    • Effect of Multiple dose Insulin on Glycaemic Control and Adiposity in Children and Adolescents with Type 1 Diabetes; a Sri Lankan Experience

      hrp0092p2-80
    • A de novo Pathogenic Heterozygous Mutation of the Insulin Receptor gene in a Patient with type A Insulin Resistance Syndrome

      hrp0092p2-81
    • Thiamine Responsive Megaloblastic Anemia Syndrome with Restrictive Cardiomyopathy: A case report

      hrp0092p2-82
    • 17q12 Deletion and a Family History of Diabetes

      hrp0092p2-83
    • An Unusual Presentation of Type 1 Diabetes

      hrp0092p2-84
    • Clinical Characteristics and Treatment Outcomes in Patients with Autoantibody-negative Ketosis-prone Diabetes

      hrp0092p2-85
    • Factors Influencing the Formation and Support of the Motivation to Self-control of Adolescents with Type I Diabetes Mellitus

      hrp0092p2-86
    • Glycemic Control in Egyptian Adolescent Girls with Type 1 DM

      hrp0092p2-87
    • A Qualitative Study Investigating the Experiences of Using Solution Focused Therapy in a Paediatrics Diabetes Team

      hrp0092p2-88
    • The Prevalence of Chronic Kidney Disease in Children and Adolescents with Type 1 Diabetes Mellitus in The Republic of Uzbekistan

      hrp0092p2-89
    • Neonatal Diabetes in Two Siblings with Foxp3 Variant

      hrp0092p2-90
    • A Novel Variant of the WFS1 Gene with Dominant Inheritance Causing Wolfram-like Syndrome

      hrp0092p2-91
    • An Impaired Lipid Profile is a Sign of Reduced Insulin Sensitivity in Children and Adolescents at Type 1 Diabetes Onset

      hrp0092p2-92
    • The Growth Hormone Treatment and Carbohydrate Metabolism in Children Born Small for Gestational Age

      hrp0092p2-93
    • Empirical Sulphonyurea in Neonatal Diabetes: Results from a aTertiary Care Centre

      hrp0092p2-94
    • Diabetes Mellitus, Severe Acanthosis Nigricans and Short Stature: a Rare Association in Chinese Children

      hrp0092p2-95
    • Evaluation of Celiac Disease Antibodies and 25-OH Vitamin D in Type 1 Diabetic Patients

      hrp0092p2-96
    • Does Commencing on an Insulin Pump Improve Glycaemic Control in Paediatric Patients?

      hrp0092p2-97
    • Prevalence of Neonatal Macrosomia (NM) and Its Relation to Hypoglycaemia (NH) in Normoglycemic Versus Dysglycemic Pregnant Women.

      hrp0092p2-98
    • A Case of Neonatal Diabetes Due to Newly Defined Mutation in the GLIS 3 Gene

      hrp0092p2-99
    • Hypertriglyceridemia as a Complication of Severe Diabetic Ketoacidosis in Newly Diagnosed Diabetes - A case report

      hrp0092p2-100
    • Evaluation of the Effect of Knowledge Levels of Adolescents Diagnosed with Type 1 Diabetes Melllitus on Hba1c and Life Quality Score

      hrp0092p2-101
    • Flash Glucose Monitoring System Versus Blood Sugar Test Strips: Cost Comparison and Satisfaction During a Year in a Northern Spain Region

      hrp0092p2-102
    • Evaluation of the Association of Glutamic Acid Decarboxylase Antibody and Limbic Encephalitis in Children with Type 1 Diabetes Mellitus

      hrp0092p2-103
    • Insulin Pump Therapy Implementation in Uzbekistan

      hrp0092p2-104
  • Fat, Metabolism and Obesity
  • • Cardiopulmonary exercise testing, body composition and metabolic status in young adults after allogeneic human stem cell transplantation for hematological malignancy in childhood

      hrp0092p2-105
    • School-age Children Awareness of Seriousness of Obesity Problem, Health-related Outcomes and Effectiveness of Self-control Preventive Strategies

      hrp0092p2-106
    • Childhood Obesity and Iron Metabolism

      hrp0092p2-107
    • Effectiveness of Multidisciplinary Outpatient Approach in the Management of Paediatric Obesity

      hrp0092p2-108
    • Metabolic Syndrome in Children and Adolescents who Survived After Childhood Cancer

      hrp0092p2-109
    • Pubertal Milestones and Related Hormonal Changes Among Children with Obesity

      hrp0092p2-110
    • Osteoprotegerin and Metabolic Status in Children with Obesity

      hrp0092p2-111
    • Identification of a Novel Heterozygous Missense Mutation in Low-density Lipoprotein Receptor Gene (LDLR) p.(Met652Thr) in an Emirati Family with Familial Hypercholesterolaemia (FH), Observed Genotype-phenotype Correlations and Pharmacotherapeutic Approaches

      hrp0092p2-112
    • Prevalence and Correlation of Non Alcoholic Fatty Liver Disease (NAFLD) with Serum Alanine Aminotransferase (ALT) Levels in Obese Indian Children

      hrp0092p2-113
    • Five Years' Follow-up of the Effect of Sex Steroid Hormone on Lipid and Glucose Metabolism in Girls with Turner Syndrome

      hrp0092p2-114
    • The Prevalence of Severe Obesity and Related Comorbidities has Increased During the Last Decade Among Children and Adolescents Referred for Evaluation at the Obesity Clinic

      hrp0092p2-115
    • Nonalcoholic Fatty Liver Disease in Pediatric Obese Patients

      hrp0092p2-116
    • Trends in Childhood Obesity, Underweight and Short Stature Among Urban School Children in Romania

      hrp0092p2-117
    • Impact of a Comprehensive Program, on Prevalence of Childhood Obesity in Andalusia, Spain

      hrp0092p2-118
    • Evaluation of Fetuin-A Level and Related Factors in Obese Adolescents

      hrp0092p2-119
    • Prevalence of Obesity among Infants Presenting with Intussusception

      hrp0092p2-120
    • A Non-invasive Model for Detection of the Metabolic Syndrome in Children and Adolescents

      hrp0092p2-121
    • Insulin-like Growth Factor-1 and Binding Protein-3 in Children with Metabolic Syndrome

      hrp0092p2-122
    • Overweight, Obesity and Hypertension among Adolescents – the Impact of Immigration and a Acculturation

      hrp0092p2-123
    • Markers of Bone Metabolism in Obese Children and Adolescents

      hrp0092p2-124
    • Clinical Features and Genetic Analysis of Childhood Dyslipidemia

      hrp0092p2-125
    • Tracking Body Mass Index From Infancy into Childhood

      hrp0092p2-126
    • The bilirubin/triglycerides Ratio Predicts Changes over time in Glycated Hemoglobin in Prepubertal Healthy Children

      hrp0092p2-127
    • Is one year of Diet and Physical Activity Program for Obese Children Enough to Revert the Metabolic Disorders?

      hrp0092p2-128
    • Characterization of Adherence to Follow-up and Therapeutical Outcomes in a Large Cohort of 1300 Patients with Obesity Visited in a Specialized Tertiaty Care Center

      hrp0092p2-129
    • Severe Obesity – Much More Than an Unhealthy Lifestyle

      hrp0092p2-130
    • Serum 25-hydroxyvitamin D Levels and Insulin Sensitivity Across Pubertal Stages in Obese Children

      hrp0092p2-131
    • Association Between TSH and Metabolic Syndrome in Obese Children and Adolescents

      hrp0092p2-132
    • Primary Hyperlipidemia in Children: Experience of 11 years from a Referral Center in Vietnam

      hrp0092p2-133
    • Tumor Necrosis Factor Alpha in Metabolic Syndrome Development in Children

      hrp0092p2-134
    • Clinical and Cytogenetic Analysis on Two Chinese Familial Cases of Prader-Willi Syndrome with Multiple Affected Patients

      hrp0092p2-135
    • Insulin Resistance and Impaired Glucose Tolerance in Overweight/Obese Adolescents Attending an Obesity Clinic in Belgium

      hrp0092p2-136
    • Clinical Characteristics and Response to Growth Hormone Treatment in Patients with Prader-Willi Syndrome

      hrp0092p2-137
    • A Rapid Instrument for Diagnosis and Screening of Pediatric Obesity and its Complications: The Neck Circumference

      hrp0092p2-138
    • The Prevalence of Elevated Blood Pressure and Hypertension in Korean Adolescents, based on the Guidelines of Endocrine Society and American Academy of Pediatrics

      hrp0092p2-139
    • Pedobesity: Development of Intelligent Multi-level Information Systems and Specialized Artificial Intelligence Algorithms for Personalized Management of Obesity in Childhood and Adolescence

      hrp0092p2-140
    • Metabolic Syndrome Risk Assessment in Indian children and Adolescents

      hrp0092p2-141
    • Vitamin D Status in Obese Children and its Relationship with Leptin and Adiponectin

      hrp0092p2-142
  • Fetal, Neonatal Endocrinology and Metabolism (to include Hypoglycaemia)
  • • Two Siblings with Tyrosinaemia Type 1 and Transient Hyperinsulinaemic Hypoglycaemia

      hrp0092p2-143
    • Glucagon Therapy in Preterm Infants with Hyperinsulinemic Hypoglycaemia

      hrp0092p2-144
    • Neonatal Hypo-ketotic Hypoglycemia Secondary to Transient Hyperinsulinism. Diazoxide Responsiveness and Experience with Fasting Test after Treatment Withdrawal

      hrp0092p2-145
    • Severe Neonatal Hyperparathyroidism Due to a Novel Homozygous Mutation of the Calcium-Sensing Receptor (CaSR)

      hrp0092p2-146
    • A Rare Cause of Pediatric Hypoglycemia in a Boy: A Malignat Insulinoma

      hrp0092p2-147
    • Neonatal Hyperglycemia

      hrp0092p2-148
    • Clinical and Genetic Characteristics of Patients with Hyperinsulinaemic Hypoglycaemia Diagnosed and Treated at a Tertiary Endocrine Center, a part of the ENDO-ERN

      hrp0092p2-149
    • Relations of O2 Supplementation to Blood Serum Insulin-like Growth Factor-II / Insulin-like Growth Factor-binding Protein-3 Ratios in the Not-life-threatened Human Newborn; Role of Oral-enteral Caloric Intake Beyond Axillary Temperature

      hrp0092p2-150
    • Refractory Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Imprinting Centre 1 Gain of Methylation: Severity Discordant to Genotype

      hrp0092p2-151
    • Congenital Hyperinsulinism due to Compound Heterozygous Mutations in ABCC8 Fully Responsive to Diazoxide Therapy

      hrp0092p2-152
  • GH and IGFs
  • • Criteria for First-Year Growth Response to Growth Hormone Treatment in Prepubertal Children with Growth Hormone Deficiency: Do they Predict Final Height Outcome?

      hrp0092p2-153
    • Determinants of the Peak GH Response of the Glucagon Stimulation Test in Slowly Growing Children

      hrp0092p2-154
    • First Reported Egyptian Sibs with the Rare Laron Syndrome

      hrp0092p2-155
    • Growth Hormone Monotherapy Versus Combined GH and LHRH Analog in 2 Sisters with Short Stature, Early Pubertal Development, and Advanced Bone Age (BA)

      hrp0092p2-156
    • Long-Term Follow-Up of Three Patients with Isolated Growth Hormone Deficiency Type IA Withsustained Growth Response to rhGH

      hrp0092p2-157
    • Clinical and Genetic Characteristics of Eleven Korean Patients with Hypochondroplasia and Outcomes of Growth Hormone Therapy

      hrp0092p2-158
    • Growth Hormone Treatment Adherence in Latin American Patients: 2-Year Real World Data from the Easypod™ Connect eHealth Platform

      hrp0092p2-159
    • Metabolic Outcome in Adolescents with Growth Hormone Deficiency During Transition Phase

      hrp0092p2-160
    • The Influence of Pituitary MRI Findings on Clinical Presentation and Growth in GH-Treated Children with Congenital Hypopituitarism

      hrp0092p2-161
    • Metabolic Effects of Growth Hormone Treatment in Short Prepubertal Children: A Double-Blinded Randomized Clinical Trial

      hrp0092p2-162
    • Growth Response in Short Preterm- Born Children Small for Gestational Age in First Year of Growth Hormone Treatment

      hrp0092p2-163
    • Brain Magnetic Resonance Imaging in Children with Isolated Growth Hormone Deficiency and Idiopathic Short Stature Diagnoses

      hrp0092p2-164
    • The Clinical Significance of Post-Sleep Growth Hormone Levels in the Diagnosis of Growth Hormone Deficiency

      hrp0092p2-165
    • Prediction of the First-Year Response to Growth Hormone Treatment in Prepubertal Korean Children with Idiopathic Growth Hormone Deficiency: Analysis of Data from the LG Growth Study Database

      hrp0092p2-166
    • Adherence and Long-Term Outcomes of Therapy in Pediatric Subjects in Argentina using Easypod™ Electromechanical Device for Growth Hormone Treatment: The Phase IV Multicentre Easypod™ Connect Observational Study (ECOS)

      hrp0092p2-167
    • Abstract unavailable

      hrp0092p2-168
    • Experience of Growth Hormone Therapy in Two Cases with Congenital Adrenal Hypoplasia

      hrp0092p2-169
    • Growth Hormone Therapy in Patients with SGA Short Stature Improves Body Composition by Increasing Muscle Mass and Bone Mineral Density Rather Than Decreasing Fat Mass

      hrp0092p2-170
    • Final Height in GH-deficient Paediatric Patients: A Nationwide Experience

      hrp0092p2-171
    • Differences of Efficiency of Treatment of Isolated Growth Hormone Deficiency and Panhypopituitarism in Children in Real Clinical Practice

      hrp0092p2-172
    • Implementation of a Growth Disorders Related Twinning Program in Pediatric Endocrinology – is it Necessary and Feasible?

      hrp0092p2-173
    • Empirical Change of Practice in Treatment of Growth Hormone Deficient Patients in Order to Improve 1st Year Height Outcome

      hrp0092p2-174
  • Growth and Syndromes (to include Turner Syndrome)
  • • The Impact of Growth Hormone Treatment in Patients with Noonan Syndrome and Growth Hormone Deficiency

      hrp0092p2-175
    • Efficacy and Safety of Growth Hormone (GH) in the Treatment of Children with Hypochondroplasia (HCH): Comparison with a Historical Cohort of Untreated Children with HCH

      hrp0092p2-176
    • Five Novel Variants of KMT2D/KDM6A Found in Seven Chinese Patients with Kabuki syndrome and a Literature Review of 39 Patients Reported in China

      hrp0092p2-177
    • Adult Height of Patients Enrolled in PATRO Children, An Ongoing Observational Study of the Long-term Safety And Effectiveness Of Omnitrope®

      hrp0092p2-178
    • Unusual Case of Patient with Klinefelter Syndrome with Shox Deletion Born to the Mother with Leri-weill Dyschondrosteosis

      hrp0092p2-179
    • Sudden Death in an Infant Attributed to Arrhythmia Associated with Beckwith-Wiedemann Syndrome due to Hypomethylation of Imprinting Control Region 2 on Chromosome 11p15.5

      hrp0092p2-180
    • A Novel Case Of Paternal Isodisomy for Chromosome 7 Associated with Overgrowth

      hrp0092p2-181
    • Auditory Phenotypes and Dynamics of Hearing Thresholds in 246 Turner Syndrome Females

      hrp0092p2-182
    • The Prevalence of Celiac Disease (CD) in Children with Type 1 Diabetes Mellitus (T1D); Does CD Adversely Affect Linear Growth in these Children?

      hrp0092p2-183
    • Effect of Gonadotropin-Releasing Hormone Agonists on Auxological Outcomes of Korean Boys with Central Precocious Puberty and Early Puberty

      hrp0092p2-184
    • Premature Infants Born Small to Gestational Age: Growth Dynamics in the First 5 Years of Life

      hrp0092p2-185
    • Clinical Features in a Patient with Turner Syndrome and Pericentric Inversion of Chromosome 9

      hrp0092p2-186
    • "Transition Readiness in Girls and Young Women with Turner Syndrome – are they Less Ready?" Associations between Transition Readiness and Diagnosis

      hrp0092p2-187
    • Clinical and Molecular Genetic Characterizations of Five Patients Harboring Mutations in the GNAS Gene: A Case Series and Literature Review

      hrp0092p2-188
    • Anophthalmia, Micrognathia, Combined Pituitary Hormone Deficiency, Severe Growth Retardation and Liver Dysfunction Induced Levothyroxine Sodium Powder in a Boy with Microdeletion of 14q22q23

      hrp0092p2-189
    • Growth Hormone Therapy in Patients with Noonan Syndrome

      hrp0092p2-190
    • The First Case of Genetically Diagnosed Cantu´ Syndrome in China with Mutation in ABCC9

      hrp0092p2-191
    • Shox-Haploinsufficiency Intra-Familial Phenotipic Variability and the Impact on Final Height: Report of a Pedigree

      hrp0092p2-192
    • Linear Growth of Children with Celiac Disease (CD) after the First Two Years on a Gluten-Free Diet (GFD); A Controlled Study

      hrp0092p2-193
    • Growth Hormone Treatment Adherence in Patients from an Emerging Economy Country: 1-Year Real-World Data from the Easypod™ Connect Ehealth Platform

      hrp0092p2-194
    • The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation

      hrp0092p2-195
    • Klinefelter Syndrome Associated with Short Stature Due to Iatrogenic Cushing

      hrp0092p2-196
    • Extending the Phenotype and Genotype of Okur–Chung Neurodevelopmental Syndrome

      hrp0092p2-197
    • Evaluation of Diagnosis, Follow-up and Treatment Results of Growth Hormone in Rare Diseases; 10 Year Single Center Experience

      hrp0092p2-198
    • Growth failure in children with sickle cell anemia

      hrp0092p2-199
    • Endocrine Features of Schaaf-Yang Syndrome. Case Report

      hrp0092p2-200
    • Papillary Thyroid Cancer in a 17-Years Old Girl with a Late-Diagnosed Turner Syndrome

      hrp0092p2-201
    • The Applicability of the NH-Clinical Scoring System on Diagnosis of Iranian Children with SRS

      hrp0092p2-202
  • Multisystem Endocrine Disorders
  • • Clinical Manifestations & Molecular analysis of Thirteen Palestinian Families with Sanjad Sakatti Syndrome Revealing a Common Deletion Founder Effect and Another Two Novel Mutations

      hrp0092p2-203
    • Electromagnetic Fields Exposure in Adolescents: A Survey in 11-14 y Old Greek Students

      hrp0092p2-204
    • Subcutaneous Ossifications in Children - Think About AHO!

      hrp0092p2-205
    • Growth Outcomes in Growth Hormone Treated Indian Children with Celiac Disease

      hrp0092p2-206
    • Functional Ovarian and Thyroid Disturbances in a Group of Adolescents with Insulin Dependent Diabetes Mellitus and Vitamin D Deficiency

      hrp0092p2-207
    • Autoimmune Polyendocrine Sydrome Type I: A Neuroendocrine Multi-Systemic Disease with a Variable Expressivity

      hrp0092p2-208
    • Endocrine Complications of Patients with Hepatic Type of Glycogen Storage Disease

      hrp0092p2-209
    • Autoimmune Thyroiditis and Autoimmune Hepatitis Presenting at Onset of Type 1 Diabetes (T1D)

      hrp0092p2-210
    • Ulnar Mammary Syndrome - A Case Report

      hrp0092p2-211
    • Unusual Ovary Formation in a Girl with McCune-Albright Syndrome

      hrp0092p2-212
    • Heart Rate Variability in Adolescent Polycystic Ovary Syndrome Greek Patients

      hrp0092p2-213
    • Celiac Disease and Endocrine Autoimmunity in Children and Adolescents

      hrp0092p2-214
    • Intestinal Ganglioneuromatosis as First Manifestation of Multiple Endocrine Neoplasia 2B in a Premature Girl

      hrp0092p2-215
    • Hypothyroidism in a Two and a Half Year-Old Boy with an Angelman Syndrome (AS)

      hrp0092p2-216
  • Pituitary, Neuroendocrinology and Puberty
  • • Effect of Testosterone Enanthate Therapy on Adult Height, Genital Maturation, and Bone Mineral Density in Children and Adolescents with Male Hypogonadotropic Hypogonadism

      hrp0092p2-217
    • The Difference of Body Mass Index (BMI) Score Before and After Gonadotropin-Releasing Hormone Agonist (GnRHa) Treatment in Central Precocious Puberty Girls

      hrp0092p2-218
    • Aromatase Inhibitor Treatment in Patient with Beta-Human Chorionic Gonadotrophin Secreting Tumor and Gonadotropin-Independent Precocious Puberty

      hrp0092p2-219
    • Normalized Pubertal Tempo of Maturation and Pubertal Height Gain in Girls with MPHD, Using a Physiological Treatment Approach with Natural Estrogens & rhGH

      hrp0092p2-220
    • The Case of Congenital Hypopituitarism Due to Mutation POU1F1 in 3 Azerbaijani Newborn Boys

      hrp0092p2-221
    • Case Report of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) Caused by Rare AVPR2 Gene Active Mutation

      hrp0092p2-222
    • Long Term Effects of GnRH Agonist Therapy on BMI in Girls with Idiopathic Central Precocious Puberty

      hrp0092p2-223
    • To Whom Should Central Nervous System Imaging be Performed in Girls with Central Precocious Puberty (CPP)?

      hrp0092p2-224
    • Unusual Presentation of McCune-Albright Syndrome in a 10-Year-Old Girl

      hrp0092p2-225
    • Endocrine Transition of Care From Pediatric to Adult Medicine in Adolescents and Young Adult Survivors of Childhood Brain Tumour. Experience at Hôpital Universitaire Necker-Enfants Malades and Hôpital Universitaire La Pitié-Salpêtrière – A Follow-Up Study of the 2010-2015 Cohort

      hrp0092p2-226
    • Screening of Central Precocious Puberty (CPP) in Females: Efficacy of Morning Unstimulated Luteinizing Hormone (mLH) Levels

      hrp0092p2-227
    • Near Adult Height According to Genetic Target and Absence Of Craniofacial Bone Fibrous Dysplasia in a Girl With Mc Cune Albright Syndrome and Growth Hormone Excess: 12.6 Years Follow-up

      hrp0092p2-228
    • Normalized Pubertal Tempo of Masculinisation and Pubertal Height Gain in Boys With MPHD, Using a Physiological Treatment Approach with Low Dose Testosterone and Adequate Dose rhGH

      hrp0092p2-229
    • The Incidence and Diagnostic Factors of Polydipsia and Polyuria: A Single Center Survey in Japan

      hrp0092p2-230
    • Macroprolactinoma Presenting with Pituitary Apoplexy Associated with Middle Cerebral Artery Infarction in an Adolescent Male

      hrp0092p2-231
    • Childhood Craniopharyngioma: Clinical Picture at Diagnosis in an Italian Multicentre Study

      hrp0092p2-232
    • Central Precocious Puberty with Herlyn-Werner-Wunderlich Syndrome: A Case Reports

      hrp0092p2-233
    • Evaluation of Clinical Features and Treatment Responses of Cases with Hyperprolactinemia

      hrp0092p2-234
    • A Case of Gonadotropin-Independent Precocious Puberty Due to Germ Cell Tumor in the Frontal Lobe

      hrp0092p2-235
    • Isolated Premature Menarche into Two Siblings with Neurofibromatosis Type 1

      hrp0092p2-236
    • Heterozygous OTX2 Deletion in a Boy with Normal Eye Development and Normal Pituitary Function

      hrp0092p2-237
    • Risk Factors for Hypogonadism in Patients with β-Thalassemia Major: A Cross-Sectional Study

      hrp0092p2-238
    • Radiation Therapy for Children with Medulloblastoma: Growth and Thyroid Sequalae

      hrp0092p2-239
    • Bone Age Determination in Girls with Early Puberty and Limitations of Adult Height Prediction: Can Automated Evaluation (BoneXpert™)be a Solution?

      hrp0092p2-240
    • Effect of Gonadotropin-Releasing Hormone Agonist Treatment on Final Adult Height in Boys with Idiopathic Central Precocious Puberty

      hrp0092p2-241
    • Evaluation of the of Alpha2-Adrenergic Receptors Stimulation Effect on Prolactin Secretion, Based on the Result of the Test with Clonidine Used in the Diagnosis of Children with Short Stature

      hrp0092p2-242
    • A Case of Severe Recurrent Hypoglycemia After Traumatic Brain Injury

      hrp0092p2-243
  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology
  • • The Evolving Role of Whole Exome Sequencing in the Diagnosis of Disorders of Sex Development (DSD)

      hrp0092p2-244
    • Etiological Structure Disorders of Sex Development 46,XY By One Center

      hrp0092p2-245
    • Comparison of Growth Status, Level of Blood Glucose and Lipid Metabolism in SGA and AGA Girls with Central Precocious Puberty

      hrp0092p2-246
    • Does the Anogenital Distance Predict Outcome of Hypospadias Repair?

      hrp0092p2-247
    • GnRH Analogues Use in Post-Pubertal Adolescents with Gender Dysphoria Causes a Reduction in Bone Density Values

      hrp0092p2-248
    • 11-Oxygenated Androgens May be Related to the Virilization of Female External Genitalia Due to the Maternal Androgen-Producing Adrenal Tumor

      hrp0092p2-249
    • High Prevalence GnRH Receptor Mutations in Russian Patients with Idiopathic Hypogonadotropic Hypogonadism

      hrp0092p2-250
    • 3β-HSD2 Deficiency Due to Compound Heterozygosity of a Missense Mutation (p.Thr259Met) and a Frameshift Deletion (p.Lys273ArgFs*7) in an Under-Virilized Infant Male with Salt Wasting

      hrp0092p2-251
    • Clinical Evaluation of Newly Developed Scoring System for DSD (DSD-SS): Association of DSD-SS With Assigned Gender in 45,X/46,XY Mosaicism

      hrp0092p2-252
    • Complexities of Diagnosis in 17-Beta-Hydroxysteroid Dehydrogenase Deficiency and Implementation of Next Generation Sequencing in Guiding Management Decisions – Case Series of Six Patients

      hrp0092p2-253
    • Paediatric Health Assistance to Transsexual Minor in the Multidisciplinary Care Unit of the Basque Country (Spain)

      hrp0092p2-254
    • A Rare Cause of 46, XX ovotesticular DSD: Tetragametic Gonadal Chimerism

      hrp0092p2-255
    • A Clinical and Cytogenetic Study of Patients with Disorders of Sex Development (DSDs) Associated with Congenital Anomalies or Recognizable Syndromes

      hrp0092p2-256
    • Physical Changes, Laboratory Parameters and Bone Mineral Density During Testosterone Treatment in Adolescents with Gender Dysphoria

      hrp0092p2-257
    • Study of Autistic Features Among Children and Adolescents with Congenital Adrenal Hyperplasia

      hrp0092p2-258
    • Differences of Sex Development with Chromosomal Mosaicism: Histological Characterization and Immunohistochemistry Markers in Gonads During Childhood

      hrp0092p2-259
    • Heterozygous CYP11A1 Mutation Associated with 46XY Disorder of Sexual Differentiation and Mild Adrenal Insufficiency

      hrp0092p2-260
    • Abstract unavailable

      hrp0092p2-261
    • Etiologic Classification of 46, XX Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results

      hrp0092p2-262
    • Novel Genotype in Two Siblings with 5-Alpha-Reductase 2 Deficiency:Different Clinical Course Due to the Time of Diagnosis

      hrp0092p2-263
    • Ethical and Familial Dilemmas of Genitoplasty Encountered in Congenital Adrenal Hyperplasia

      hrp0092p2-264
    • Hormonal Assessment of Malformation Syndromes Associated with Disorders of Sex Development: Case Series of 9 Patients

      hrp0092p2-265
    • Family Perrault Syndrome in Two Tunisian Sisters

      hrp0092p2-266
    • An Intriguing Co-Occurrence of MURCS and VACTERL Association: A Case Report and Review of the Literature

      hrp0092p2-267
    • The Effect of Vitamin D Supplementation on Androgen Levels of Adolescent Girls with Hyperandrogenism

      hrp0092p2-268
    • Pseudo-Precocious Puberty in Children Triggered by Incidental Transdermal Contamination with Topical Sex Steroids Through Parents

      hrp0092p2-269
    • Follow-up of Individuals with Gender Identity Disorders: A Long and Challenging Process

      hrp0092p2-270
    • Follow-Up of Two Similar Patients with Steroidogenic Factor-1 (SF-1/ NR5A1) Variants, in Two Different Eras

      hrp0092p2-271
    • Genetic Testing of DSD Patients in Ukraine

      hrp0092p2-272
    • Spectrum of Genital Abnormalities in Robinow Syndrome: Case Series

      hrp0092p2-273
    • MAMLD 1 Gene Mutation and 46 XY Sex Development Disorder: A Case Report

      hrp0092p2-274
    • 46,XY Complete Gonadal Dysgenesis in a Familial Case with a Rare Mutation in the Desert Hedgehog (DHH) Gene

      hrp0092p2-275
  • Thyroid
  • • Novel Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone

      hrp0092p2-276
    • Congenital Hypothyroidism: Neonatal SCREENING PROGRAM with T4 and TSH

      hrp0092p2-277
    • A 10- Year-Old Girl with Thyroid Hormone Resistance (βTHR)- Case Report

      hrp0092p2-278
    • Diagnosis of Central Congenital Hypothyroidism and Multiple Pituitary Deficiencies Through a Neonatal Screening Program

      hrp0092p2-279
    • Childhood Thyroid Cancer After Radi Oiodine Therapy

      hrp0092p2-280
    • Differential Diagnosis of Euthyroid Hyperthyroxinemia

      hrp0092p2-281
    • Treatment for Graves' Disease in Children and Adolescents: A Long-Term Retrospective Study at a Single Institution

      hrp0092p2-282
    • Changes of Thyroid Function in Girls with Central Precocious Puberty After 6-Month GnRH Agonist Treatment

      hrp0092p2-283
    • Papillary Thyroid Cancer Associated with Hyperthyroidism

      hrp0092p2-284
    • Serum PTH Does not Correlate with Their Serum Calcium Levels in Children and Adolescents with Hashimoto Thyroiditis

      hrp0092p2-285
    • Management of Childhood Thyroid Nodules in Children a Large Group of Cases From a Single Center

      hrp0092p2-286
    • Bone Homeostasis in Children with Subclinical Hypothyroidism: Effects of Two-years Treatment with Levothyoxine

      hrp0092p2-287
    • The Most Frequently Seen Reason of Congenital Hypothyroidism: Iodine Loading

      hrp0092p2-288
    • Uncommon Presentations of a Common Condition: Experience from a Teaching Hospital!

      hrp0092p2-289
    • A Rare Combination- Brain Lung Thyroid Syndrome

      hrp0092p2-290
    • Investigation of Oxidative Effect in Saliva and Gingival Groove Fluids in Children with Hashimoto Thyroiditis

      hrp0092p2-291
    • Thyroid Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus

      hrp0092p2-292
    • Analysis of Diabetes-Associated Autoantibodies in Children and Adolescents with Autoimmune Thyroid Diseases

      hrp0092p2-293
    • A New Case of Thyroid Hormone Resistance α Caused by a Mutation of THRA/TRa1

      hrp0092p2-294
    • The Incidence of Congenital Hypothyroidism During the Neonatal Screening Program in the Republic of Karakalpakstan, Uzbekistan

      hrp0092p2-295
    • Progressive Thyroid Dysfunction in Infants with Down Syndrome; Trisomy 21 (DS): Effect on Linear Growth

      hrp0092p2-296
    • Evaluation of Elevated Serum Thyroid-Stimulating Hormone (TSH) in Children and Adolescents: A Single-Center Study in Uruguay

      hrp0092p2-297
    • Neonatal Hyperthyroidism: Our Centre's Experience

      hrp0092p2-298
    • Epidemiological Aspects of Pediatric Thyroid Disorders in Western Ukraine

      hrp0092p2-299
    • The Encephalopathy as Complication of Hashimoto Thyroiditis in Children: A Wide Variety of Clinical Manifestations

      hrp0092p2-300
    • Acute-Onset Peripheral Polyneuropathy in a 12-Year-Old Girl Due to Hashimoto Thyroiditis: Traps in the Diagnosis

      hrp0092p2-301
• Poster Category 3
• • Adrenals and HPA Axis
  • • A Case of Cushing Syndrome in a Wilms' Tumour

      hrp0092p3-1
    • A Rare Cause of Primer Adrenal Insufficiency: NROB1 (DAX1) Mutation

      hrp0092p3-2
    • A 46, XX Patient with 21-OHD Diagnosed During the Etiologic Workup of Male Infertility

      hrp0092p3-3
    • A Female Infant with Severe Salt-Wasting due to Aldosterone Synthase Deficiency, Initially Mimicking Adrenal Insufficiency

      hrp0092p3-4
    • Can Early Prenatal Prednisone Treatment Reduce Virilization of CAH Female Newborn?

      hrp0092p3-5
    • Clinical Characteristics and Etiological Diagnosis of Premature Pubarche Among 55 Children

      hrp0092p3-6
    • Rare Case of Cortisol Producing Tumour in 14 Years Old Girl

      hrp0092p3-7
    • Typical Phenotype of Isolated Aldosterone Synthetase (AS) Deficiency in two Infants with Heterozygous AS Gene Mutation: Dilemma for Diagnosis

      hrp0092p3-8
    • Late Onset 11 Beta Hydroxylase Deficiency: Two Cases

      hrp0092p3-9
    • An Unusual Testicular Adrenal Rest Tumor localization in a 15-Year-Old Boy with Congenital Adrenal Hyperplasia

      hrp0092p3-10
    • Primary Adrenal Insufficiency in Sudanese Children (Clinical Presentation, Etiology and Diagnostic Challenges)

      hrp0092p3-11
    • Clinical Follow-Up of a Novel NR0B1 Mutation in a Case of Adrenal Hypoplasia Congenital

      hrp0092p3-12
    • Genotype and Phenotype, Growth Outcome in 33 Korean Patients with 21-Hydroxylase Deficiency

      hrp0092p3-13
    • One Case Report of Uighur Girl with Cushing Syndrome

      hrp0092p3-14
    • Nephrotic Syndrome Developed in a Girl With Lipoid Adrenal Hyperplasia due to StAR Gene Mutation – First Report

      hrp0092p3-15
    • Pneumocystis Jiroveci Pneumonitis Complicating Neonatal Cushing's Syndrome - the Therapeutic Dilemma

      hrp0092p3-16
    • Newborn Screening for Congenital Adrenal Hyperplasia: Should we Worry more about False Positives or False Negatives?

      hrp0092p3-17
    • The Unusual Adverse Side Effects of Super-Potent Topical Steroids

      hrp0092p3-18
    • A Case with Central Adrenal Insufficiency and Early Onset Obesity: Proopiomelanocortin Deficiency

      hrp0092p3-19
    • Short Synacthen Test in Children at Sultan Qaboos University Hospital; Reviewing the Sampling Times

      hrp0092p3-20
    • Pheochromocytoma in Children: A Case Report

      hrp0092p3-21
    • A Case with Congenital Adrenal Hyperplasia Diagnosed by Malnutrition

      hrp0092p3-22
    • Recurrent Hypoglycemia-Not Every Low Sugar is Hyperinsulinemia

      hrp0092p3-23
    • Clinical Characteristics and Genetic Analysis in one Patient with Congenital Lipoid Adrenal Hyperplasia

      hrp0092p3-24
    • Unusual Association: Allgrove Syndrome and Hypopituitarism

      hrp0092p3-25
    • Title: Long-Term Outcome of Congenital Adrenal Hyperplasia Patients at KFSHRC-Saudi Arabia. Tertiary Center Experience

      hrp0092p3-26
    • A Boy with Adrenal Hypoplasia Congenita without External Genital Abnormalities

      hrp0092p3-27
  • Bone, Growth Plate and Mineral Metabolism
  • • Linear Growth in Children with COW Milk Allergy and their Response to Hypoallergenic Diet; Significant Catch-Up in the First 6 Months

      hrp0092p3-28
    • Extreme Hypercalcaemia: Watch for Glycogen Storage Disease Type 1a with Hyperinsulinism

      hrp0092p3-29
    • ENPP1 Hypophosphatemic Rickets in a 3.6 Years Old Italian Child

      hrp0092p3-30
    • A Case Study of X-linked Hypophosphataemia: The Effect of Conventional Therapy from Childhood to Adulthood in Saudi Arabia

      hrp0092p3-31
    • A Chinese Girl Suffered Both Osteogenesis Imperfecta and Mucopolysaccharidosis: Trio WES Could Tell us More

      hrp0092p3-32
    • In Case of Osteogenesis Imperfecta Transmission in Pregnancy: Check Vitamine D and Calcium Status of the Mother

      hrp0092p3-33
    • Study of Response to Vitamin D Replacemet in North Korean Refugee Children and Korean Children

      hrp0092p3-34
    • Pseudohypoparathyroidism: Four Cases Reports

      hrp0092p3-35
    • A Case of Robinow Syndrome

      hrp0092p3-36
    • Abstract unavailable

      hrp0092p3-37
    • Mild Hypophosphatasia in a Family with a Novel Mutation in the ALPL Gene

      hrp0092p3-38
    • Uncommon Association of Hypoparathyroidism and Rendu-Osler Syndrome

      hrp0092p3-39
    • Barakat Syndrome (HDR Syndrome): Case Report

      hrp0092p3-40
    • Myelofibrosis in Severe Vitamin D Deficiency Rickets: A Case Report

      hrp0092p3-41
    • Congenital Hyperinsulinism in Kosova

      hrp0092p3-42
    • About a Case of Neonatal Hypocalcemia

      hrp0092p3-43
    • Rare Case Report: Asymptomatic Hypercalcemia in Children with Lupus Nephritis Complicated with Parathyroid Adenoma

      hrp0092p3-44
    • Acute Lymphoblastic Leukemia;Atypically Presenting with Sever Hypercalcemia in a Palestinian Child

      hrp0092p3-45
    • Growth Hormone Treatment of a Patient with X-Linked Hypophosphatemic Rickets Caused by PHEX Mutation: Effects on Linear Growth

      hrp0092p3-46
  • Diabetes and Insulin
  • • Serum Catecholamines in Children With Type 1 Diabetes Mellitus

      hrp0092p3-47
    • Oral Glucose Tolerance Test (OGTT) as a Useful Tool for Early Diagnosis of Type 2 Diabetes Mellitus and Prediction of Metabolic Risks in Children and Adolescents

      hrp0092p3-48
    • Significance of the Early Marker of Nephrine Diabetic Nephropathy of the Uzbek Nationality with the First Type of Diabetes Mellitus

      hrp0092p3-49
    • Hybrid Diabetes with Good Response to Metformin in an Adolescent with Polyglandular Polyendocrinopathy (APS2)

      hrp0092p3-50
    • Treatment of Hfd Induced Diabetes with Combination of Natural Product and Metformin in Rats

      hrp0092p3-51
    • Off Label use of CGM in a Pediatric Patient with Type 1 Diabetes Mellitus Under the Age of 2

      hrp0092p3-52
    • A Case of Congenital Hyperinsulinism due to ABCC8 Mutation: A Challenge to Diagnosis, Management, and Treatment

      hrp0092p3-53
    • Relationship Between Chloride Infusion and Base Excess in Initial Treatment of Pediatric Diabetic Ketoacidosis

      hrp0092p3-54
    • The Role of Patient Adherence to Insulin Pump Therapy with Long-Term Treatment of Type 1 Diabetes

      hrp0092p3-55
    • Long-Term Honeymoon Period in Type 1 Diabetes: True Diagnosis MODY5; New Mutation of HNF1B

      hrp0092p3-56
    • Prevalence of Celiac Disease (CD) and Autoimmune Thyroid Dysfunction (AITD) in Indian Children with Type 1 Diabetes

      hrp0092p3-57
    • Mauriac's Syndrome: A Complication of Poorly Controlled Type 1 Diabetes Mellitus in Childhood and Adolescence

      hrp0092p3-58
    • Acute and Chronic Complications in Pediatric Patients with Diabetes Mellitus Type 1. Findings in A Country with Limited Resources and High Incidence of Terminal Renal Disease

      hrp0092p3-59
    • Clinical Characteristics and Literature Review of Special Type of Diabetes Mellitus- Thiamine-Responsive Megaloblastic Anemia Syndromein Infant with Acute Ischemic Stroke

      hrp0092p3-60
    • The Effect of Fibroblast Growth Factor 23 on Serum Phosphorus Level in Children with Diabetic Ketoacidosis

      hrp0092p3-61
    • What Does the Insulin Pump Change in Children with Type 1 Diabetes? One-Year Clinical Follow-Up

      hrp0092p3-62
    • Severe Heart Disease can Cause Diabetes Mellitus Even in Younger Age: Case Reports of Two Japanese Adolescent Boys

      hrp0092p3-63
    • De Novo Mutation of ABCC8 Gene in a Child with MODY Developed at 25 Months of Age

      hrp0092p3-64
    • Insulin-Induced Oedema in a Child with Newly Diagnosed Diabetes Mellitus

      hrp0092p3-65
    • Familial Hypercholesterolaemia as a Cause of Dyslipidemia in Patient with Type 1 Diabetes

      hrp0092p3-66
    • What has Changed in Type 1 Diabetes Mellitus Cases in the Last Eight Years? A Single Center Experience

      hrp0092p3-67
    • Seasonal Variation and Epidemiological Parameters in Children from Western Greece with Type 1 Diabetes Mellitus (T1DM)

      hrp0092p3-68
    • An 8-Year-Old Boy with Down Syndrome who has had a History of Transient Hyperinsulinemia and was found to have Type 1 Diabetes During ALL Treatment

      hrp0092p3-69
    • Indicators of Caries Risk in Children with Type 1 Diabetes Mellitus

      hrp0092p3-70
    • Vitamin D Status in Egyptian Children with Newly-Diagnosed Type 1 Diabetes and its Relation to Autoimmune Destruction of Pancreatic Beta Cells

      hrp0092p3-71
    • Hematologic Indices Indicating Platelets Activity in Children with Type 1 Diabetes

      hrp0092p3-72
    • The Prevalence of Hypertension and its Relationship to Glycemic Control in Children with Type 1 Diabetes Mellitus

      hrp0092p3-73
    • Does Metformin Therapy Prolong the Honeymoon Period in Obese Adolescent with Hybrid Diabetes?

      hrp0092p3-74
    • A 16-Year-Old Girl with Prader-Willi Syndrome and Type 2 Diabetes Mellitus

      hrp0092p3-75
    • Extra Attention to be Paid When Looking After Boys with Type 1 Diabetes Mellitus in Oman

      hrp0092p3-76
    • Factors Affecting the Preservation of C-Peptide Secretion in Egyptian Children with Type 1 Diabetes

      hrp0092p3-77
    • Prevalence of Fatty Liver in Children with Type 1 Diabetes Mellitus Attending Diabetes Clinic of Alexandria University Children's Hospital

      hrp0092p3-78
    • Hyperinsulinemia as A Consistent Feature in The Extremely Rare Donohue Syndrome

      hrp0092p3-79
    • A Real-Life Experience with a New Insulin Co-Formulation Degludec/Aspart for one Year in Poorly Controlled Children and Adolescents with Type 1 Diabetes

      hrp0092p3-80
    • Cerebellum Malacia Lesions as a Result of Severe Diabetic Ketoacidosis in 12 Month Old Patient

      hrp0092p3-81
    • Assessment of Testicular Volume by Ultrasound in Children and Adolescents with Type 1 Diabetes

      hrp0092p3-82
    • Diabetes Mellitus in a 16-Year-Old Boy Developing Multiple Neuro-Endocrine Dysfunctions in the Course: Is it Type 1 Diabetes or Wolfram Syndrome, or Both?

      hrp0092p3-83
    • A Low-Carbohydrate Diet Improves Metabolic Control in a Type 1 Diabetic Child Without Side Effects

      hrp0092p3-84
    • To Find Prevalence of Type 1 with Autoimmune Thyroid Disorders, Age, Duration, Thyroid Antibodies, Growth and Glycemic Variability in Indian Scenario

      hrp0092p3-85
    • Clinical Profile of Paediatric Patients with type 1 Diabetes Mellitus at a Tertiary Health Care Center in the Oriental Region of Northeastern Morocco

      hrp0092p3-86
    • Comprehensive Analysis of HLA System Class II DRB1 in Children with Insulin Dependent Diabetes Mellitus in the North Azerbaijan and Iranian Azerbaijan

      hrp0092p3-87
    • A Case of Type 2 Diabetic Adolescent With Sleep Apnea who was Successfully Stopped Metformin After Adenotonsillectomy

      hrp0092p3-88
    • A Mitophagic Response to iron Overload-Induced Oxidative Damage Associated with the PINK1/Parkin Pathway in Pancreatic Beta Cells

      hrp0092p3-89
    • A Management Challenge of Acute Viral Hepatitis A in a Child Presented with DKA as a First Presentation

      hrp0092p3-90
    • Association of Type 1 Diabetes and Celiac Disease In Child

      hrp0092p3-91
    • Case of Family Neonatal Diabetes with KCNJ11 Gene Mutation: Dynamics Monitoring

      hrp0092p3-92
    • Severe and Inaugural Diabetic Ketoacidosis in Children: Experience of a Pediatric Tunisian Department

      hrp0092p3-93
    • Role of Renal Scintigraphy as an Early Predictor of Chronic Renal Damage in Children and Adolescents with Type1 Diabetes

      hrp0092p3-94
    • Changes in the Microbiome of Pre-Type 1 Diabetic Children

      hrp0092p3-95
  • Fat, Metabolism and Obesity
  • • Assessment of Cardiac Function in Obese Children and Adolescents with Metabolic Syndrome

      hrp0092p3-96
    • Metabolic Syndrome in Adults with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

      hrp0092p3-97
    • High Allostatic Load in Children with Excess of Weight

      hrp0092p3-98
    • "Influence of Eating Habits, Sleep Patterns and Physical Activity on Anthropometric Variables and Body Composition in Children with Obesity"

      hrp0092p3-99
    • An Infant with Severe Hypertriglyceridemia: Acute and Long-Term Management in the Paediatric Population

      hrp0092p3-100
    • BigO: The use of New Technologies for the Management of Childhood Obesity – A Clinical Pilot Study

      hrp0092p3-101
    • Obesity and Insulin Resistance: Differences Between Pubertal and Prepubertal Children

      hrp0092p3-102
    • Relationship Between 25-Hydroxyvitamin D with Adiposity Assessed by Body Mass Index, Serum Glucose and Lipids Levels in Korea: A Cross-Sectional Analysis

      hrp0092p3-103
    • Treating Paediatric Morbid Obesity using the Multidisciplinary Intensive Inpatient Approach

      hrp0092p3-104
    • The Interaction Between Lipids Regulatory Genes Polymorphism and Obesity on Cardiometabolic Risk Factors in Children and Adolescents

      hrp0092p3-105
    • Phenotypic and Genotypic Properties of Children with Suspicion of Monogenic Obesity

      hrp0092p3-106
    • Relation of Serum 25 Hydroxy-Vitamin Levels D3 with Body-Mass Index in Pediatric Patients

      hrp0092p3-107
    • Vitamin B12 Levels in Children After Metformin Treatment

      hrp0092p3-108
    • Follow-Up Evaluation of Clinical Markers and Inflammatory, Biochemical and Hormonal Profiles in Children with Bodyweight Problems

      hrp0092p3-109
    • Gastroduodenopathies in Obese Young People

      hrp0092p3-110
    • Seven Methods of Indicating Childhood Metabolic Syndrome

      hrp0092p3-111
    • Insulin Resistance in Children and Adolescents with Exogen-Constitutional Obesity

      hrp0092p3-112
    • Severe Hypernatremia Revealing A Rohhad-Net Syndrome

      hrp0092p3-113
    • Rare Case of Acquired Generalized Lipodystrophy in A 14-Year Old Patient

      hrp0092p3-114
    • Gender-Based Differences in the Clustering of Metabolic Syndrome Factors in Children and Adolescents

      hrp0092p3-115
    • Fat Mass Index and Fat-free Mass Index Percentiles in Healthy Spanish Adolescents

      hrp0092p3-116
    • Comparison of Different Criteria for the Definition of Insulin Resistance and Its Relation with Metabolic Risk in Overweight and Obese Adolescents

      hrp0092p3-117
    • Somatostatine Analogue in Hypothalamic Obesity

      hrp0092p3-118
    • ESPE 2019. Physical Activity, Food and Metabolic Risk in Children and Adolescents

      hrp0092p3-119
    • Toward a Simple Marker of Hepato-Visceral Adiposity and Insulin Resistance:The Z-Score Change from Weight-at-Birth to BMI-in-Childhood

      hrp0092p3-120
    • Associations Between Lipid Parameters and Insulin Resistance in Obese Adolescents

      hrp0092p3-121
    • The Characteristic of Thyroid Status in Overweight and Obese Young People with Insulin Resistance

      hrp0092p3-122
    • Validity of Non-High-Density Lipoprotein Cholesterol for Detecting Dyslipidemia Among Korean Adolescents

      hrp0092p3-123
    • Early Onset Monogenic Obesity: Two Cases with Homozygous Mutation in Lepr Gene

      hrp0092p3-124
    • Fasting C-Peptide: A Useful Tool for Diagnosis of Type II Diabetes Mellitus in Overweight / Obese Adolescents Living in a Poor Resources Setting

      hrp0092p3-125
    • Metabolic Risk Assessment in Obese Children Using Hypertriglyceridemic Waist (HTGW) Phenotype. Can it be a Useful Screening Marker?

      hrp0092p3-126
    • Rosuvastatain Therapy in Children with Heterozygous Familial Hypercholesterolemia, Efficacy, and Security of Low Régimen of Therapy

      hrp0092p3-127
    • Lipid and Glucose Profiles in Obese Algerian Children and Adolescents

      hrp0092p3-128
    • Influence of Anthropometric Indices at Birth on Obesity Characteristics in School-Age Children

      hrp0092p3-129
    • Acanthosis Nigricans as a Presentation of Severe Insulin Resistance in Obese Children

      hrp0092p3-130
  • Fetal, Neonatal Endocrinology and Metabolism (to include Hypoglycaemia)
  • • Growth Prognosis of Small for Gestational Age in Korea: Risk of Early Adolescence

      hrp0092p3-131
    • Recurrent Apnea in a Boy Suffering from Congenital Hyperinsulinism in the Course of Diazoxide Treatment

      hrp0092p3-132
    • Relations of O2 Supplementation to Blood Serum Insulin-Like Growth Factor-I in the Not-Life-Threatened Human Newborn; Role of Oral-Enteral Caloric Intake Beyond Axillary Temperature

      hrp0092p3-133
    • Persistant Hypoglycemia in Children: Hyperinsulinemia

      hrp0092p3-134
    • Study Role of Biofortified Food with Vitamin B-6, B-12 and Folic Acid on Concentrations of Homocysteine and Vitamin in Urban Population

      hrp0092p3-135
    • Wearable Technology (MI Band and Yu Band) a Boon for Patients with Chronic Kidney Disease

      hrp0092p3-136
    • Case Report: A neonate with Prolonged Hypoglycemia

      hrp0092p3-137
  • GH and IGFs
  • • Factors Affecting Growth Response to Growth Hormone (GH) Therapy in Children with Short Stature and Normal GH and IGF-I Secretion and no Bone Age Delay

      hrp0092p3-138
    • Responses to Growth Hormone (GH) Therapy in Children with Short Stature with Normal GH Secretion and Slow Growth Velocity

      hrp0092p3-139
    • Assessment of Body Composition of Children with Short Stature on Growth Hormone Therapy and its Relation to Serum IGF-1

      hrp0092p3-140
    • Treatment Outcome of Growth Hormone in Turner Syndrome Children

      hrp0092p3-141
    • Pituitary Imaging in 23 Children with Growth Hormone Deficiency

      hrp0092p3-142
    • The Convulsions Maze: Epilepsy Versus Hypoglycemia

      hrp0092p3-143
    • A Case of Paediatric GH-secreting Pituitary Adenoma Apoplexy

      hrp0092p3-144
    • Final Adult Height of Children with Idiopathic Short Stature: A Multicenter Study on GH Therapy Alone Started During Peripuberty

      hrp0092p3-145
    • Growth Hormone Deficiency after Radiation Therapy for Brain Tumor How to Manage?

      hrp0092p3-146
    • Vitamin D Status in Patients with Short Stature

      hrp0092p3-147
    • Short Stature in Children in the Department of Endocrinology in the East of Morocco

      hrp0092p3-148
    • Local Lipoatrophy following Recombinant Human Growth Hormone Administration in Prader Willi Syndrome

      hrp0092p3-149
    • Features of Somatropin Replacement Therapy in a Patient with Floating Harbor Syndrome

      hrp0092p3-150
  • Growth and Syndromes (to include Turner Syndrome)
  • • Long-Term Follow-Up Study for a Boy with Floating–Harbor Syndrome Due to a de novo Novel Heterozygous SRCAP Mutation

      hrp0092p3-151
    • Linear Growth of Infants with Neonatal and Early Infantile Meningitis

      hrp0092p3-152
    • Prevalence of Thyroid Dysfunction and Associated Autoimmune Disorders in Young Children with Down Syndrome (DS); A Cohort Study.

      hrp0092p3-153
    • NSD2 Mutation in a Family with a New Intellectual Disability and Short Stature Syndrome: a 7.5 Years Follow-Up

      hrp0092p3-154
    • Turners Syndrome - Clinical Presentation, Genetics, Investigation and Management: A 10-Year Review

      hrp0092p3-155
    • Growth Status of Children and Adolescent Born Full Term Small-for-Gestational-Age in Korea: Data from the KNHANES-V (2010-2011)

      hrp0092p3-156
    • Bardet-Biedl Syndrome: A Case Series

      hrp0092p3-157
    • A Novel Variant of KAT6B Caused Say-Barber-Biesecker-Young-Simpson Syndrome

      hrp0092p3-158
    • Three Cases with Familial Short Stature: Leri-Weill Syndrome

      hrp0092p3-159
    • Thyroid Dysfunction in the First Year of Life in Infants with Down syndrome: Linear Growth Over 4 Years

      hrp0092p3-160
    • The Effect of Thyroxine Treatment on Linear Growth and Weight Gain in Infants and Children with Down Syndrome (DS) and High TSH Versus Children with DS and Normal Thyroid Function: A Controlled Study

      hrp0092p3-161
    • Acromesomelic Dysplasia of Maroteaux- An Extremely Rare Cause of Short Stature

      hrp0092p3-162
    • Endocrinological Evaluation of Male Patient with Floating-Harbor Syndrome –case Report

      hrp0092p3-163
    • Longitudinal Evaluation of Audiological Pattern in Turner Syndrome

      hrp0092p3-164
    • Final Adult Height in a Patient with Turner Syndrome {46, X, i(Xq)} Treated with Growth Hormone for 10 Years Compared to her Normal Dizygotic Twin Sister and Mid-Parental Height

      hrp0092p3-165
    • Growth Hormone Treatment and Puberty in Patient with Pallister-Hall Syndrome

      hrp0092p3-166
    • Bloom Syndrome in 7-Year-Old Girl Diagnosed with Short Stature

      hrp0092p3-167
    • Efficacy of Growth Hormone Treatment in a Patient with Chronic Granulomatous Disease, who Developed Acute Myeloid Leukemia after Bone Marrow Transplantation

      hrp0092p3-168
    • Schaaf-Yang Syndrome:Three Cases Report of MAGEL2 Variation and Literature Review

      hrp0092p3-169
    • Reevaluation of Congenital Growth Hormone Deficiency in Adulthood

      hrp0092p3-170
    • Prevalence and Etiology of Short Stature in Children Between 2-4 Years of Age Born SGA in a Tertiary Care Hospital in a Developing Country

      hrp0092p3-171
    • Pure Gonadal Dysgenesis with Partial Testicular Development Associated with Turner Syndrome with SRY

      hrp0092p3-172
    • A Case of Wiedemann–Steiner Syndrome with Central Precocious Puberty

      hrp0092p3-173
    • Population Prevalence of Down's Syndrome and Cardiac Complications in South Korea: Based on National Health Insurance Service (NHIS)

      hrp0092p3-174
    • McCune Albright Syndrome: Two Cases with Different Clinical Courses

      hrp0092p3-175
    • Turner Syndrome with Neonatal Revelation: Knowing How to Think About It

      hrp0092p3-176
    • Endocrine and Mammary Disorders in Girl with Cornelia De Lange Syndrome (Case History)

      hrp0092p3-177
    • Long-Term Effect of Growth Hormone Treatment on the Onset and Progression of Scoliosis in Children with Prader-Willi Syndrome

      hrp0092p3-178
  • Multisystem Endocrine Disorders
  • • Clinical and Molecular Characteristics of Pediatric Patients with Multiple Endocrine Neoplasia (MEN)

      hrp0092p3-179
    • APECED Syndrome in Childhood: Rare Clinical Presentations to Keep in Mind

      hrp0092p3-180
    • Phenotype and Clinical Course in Three Individuals with Multiple Endocrine Neoplasia Type 2A due to a RET Gene Mutation

      hrp0092p3-181
    • Two Siblings Case with Diagnosis of Autoimmune Polyglandular Syndrome Type 1

      hrp0092p3-182
    • High Demand for Collaborative Work Between Paediatric Endocrinologists in Arab Countries

      hrp0092p3-183
    • Eosinophilic Ascites: A Rare Complication of Autoimmune Polyendocrinopathy

      hrp0092p3-184
    • Final Height and Endocrine Complications in Patients with β-Thalassemia Intermedia: (TI) Our Experience in Non-Transfused Versus Infrequently Transfused Patients and Correlations with Liver Iron Content

      hrp0092p3-185
    • Variable Expressivity in Three Generation from a Colombian Family with Multiple Endocrine Neoplasia with Mutation c.482G>A (p.Gly161Asp) in the Gene MEN1 not Described in Colombia

      hrp0092p3-186
    • Difficulties in Hypothyroidism and Diabetes Treatment in Patient with GATA6 Gene Mutation –case Report

      hrp0092p3-187
    • Endocrinopathies and Linear Growth in Adolescents with β-Thalassemia Intermedia in Relation to Liver Iron Content

      hrp0092p3-188
    • Bardet-Biedl Syndrome: Not Only what but also how Matters?

      hrp0092p3-189
  • Pituitary, Neuroendocrinology and Puberty
  • • Structural Pituitary Abnormality and Dysfunction Associated with Charge Syndrome

      hrp0092p3-190
    • Hormone-Secreting Pituitary Adenomas in Children and Adolescents

      hrp0092p3-191
    • Rohhad Syndrome: Report of 2 Rare Cases From Crete-Greece

      hrp0092p3-192
    • The Pubertal Development Mode of Chinese Turner Syndrome Girls with Hormone Replacement Therapy

      hrp0092p3-193
    • Coincidental Central Precocious Puberty and Wilms Tumor

      hrp0092p3-194
    • Changes of Serum 25OHD Levels in Girls with Different Types of Central Precocious Puberty and Clinical Significance

      hrp0092p3-195
    • Precocious Pseudo-Puberty Presenting with Bilateral Ovarian Involvement and Progressing to Juvenile Granulosa Cell Tumor in a 2-Year-Old Girl

      hrp0092p3-196
    • Central Precocious Puberty in a boy with Prader-Willi Syndromeduring Growth Hormone Replacement Therapy

      hrp0092p3-197
    • A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation

      hrp0092p3-198
    • Prolactinomas in a Pediatric Population

      hrp0092p3-199
    • Extreme Short Stature and Neurological Impairment in a 17-Year-Old Male with Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation

      hrp0092p3-200
    • The Pituitary Stem Interruption Syndrome: A Neonatal Pathology not to be Ignored

      hrp0092p3-201
    • A Case Of Syndromic Hypopituitarism

      hrp0092p3-202
    • Anapylaxis Secondary to Gonadotrophin Releasing Hormone Agonist used for Precocious Puberty, Two Case Reports

      hrp0092p3-203
    • Central Diabetes Insipidus in Children with Pituitary Stalk Thickening in Two Cases

      hrp0092p3-204
    • Childhood Craniopharyngioma: A Single Centre Experience

      hrp0092p3-205
    • Unusual Cause of Hypopituitarism: A Niemann Pick Disease

      hrp0092p3-206
    • Precocious Puberty and Primary Hypothyroidism in a 6 Years and 10 Months Girl with Pituitary Macro Adenoma and Dextral Ovarian Cyst

      hrp0092p3-207
    • The Early Predictors of Serum IGF-1, DHEAS, AMH and BMP-6 in Rapidly Progressive Puberty Girls

      hrp0092p3-208
    • Pituitary Hyperplasia as a Complication of Severe Hypothyroidism due to Hashimoto's Thyroiditis Could Impair Pituitary Function

      hrp0092p3-209
    • Homozygosity for Proopiomelanocortin (POMC) Mutation in a Palestininan Child

      hrp0092p3-210
    • Peculiarities of Clinical Options for Delaying Sexual Aging in Boys-Adolescents

      hrp0092p3-211
    • Two Separate Pathologies (Coeliac Disease and Central Precocious Puberty) Associated with Catch-Up Growth in the Case of a Child Born Small for Gestational Age (SGA)

      hrp0092p3-212
    • Mitochondrial Encephalomyopathy with Acidosis and Stroke-Like Episodes in A Vietnamese Child: Clinical, Radiological and Molecular Genetic Analysis

      hrp0092p3-213
    • Central Precocious Puberty in a 2 Year-Old with No Sinister Cause

      hrp0092p3-214
    • MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty

      hrp0092p3-215
    • Family Central Early Puberty about Three Sisters

      hrp0092p3-216
  • Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology
  • • Clinical and Molecular Spectrum of Patients with Disorders of Sex Development: A Single Center Experience

      hrp0092p3-217
    • Clinical Observation of Oral Testosterone Undecanoate Treatmentforchildren with 5-Alpha-Reductase Deficiency

      hrp0092p3-218
    • Final Adult Height in SRY-Negative 46,XX Ovotesticular Differences of Sex Development Individuals

      hrp0092p3-219
    • A Rare Cause of SRY (-) 46, XX DSD: Aromatase Deficiency

      hrp0092p3-220
    • Gonadal Dysgenesis, 46 XY About 5 Familial Cases

      hrp0092p3-221
    • Research on Detecting the Dose of Estrogen in the Hormone Replacement Treatment in Girls with TS – A Retrospective Study in Single Clinical Center

      hrp0092p3-222
    • Indentification of a de Novo Mutation in the SRY Gene in a 46,XY Complete Gonadal Dysgenesis Patient with Gonadal Neoplasia and Review of Tumor Risk in 46,XY DSD Patients

      hrp0092p3-223
    • Clinical and Laboratory Characteristics of Different Various Types of Gonadal Dysgenesis in Girls with Hypergonadotropic Hypogonadism

      hrp0092p3-224
    • Evaluation of the Role of Fetuin A in Pathophysiology of Polycystic Ovarian Syndrome in Adolescents

      hrp0092p3-225
    • Rare Cause of 46,XY Sexual Development Disorder: 17β-Hydroxysteroid Dehydrogenase Type 3 Deficiency

      hrp0092p3-226
    • Persistent Elevation of Gonadotropins in a Girl with Aromatase Deficiency Despite Adequate Estradiol Supplementation- A Case for Reset Hypothalamic-Gonadal Axis

      hrp0092p3-227
    • Comparison of Classical and Non-Classical Turner Syndrome at NICH Karachi

      hrp0092p3-228
    • Primary Amenorrhea Revealing Leydig Cell Hypoplasia

      hrp0092p3-229
    • Novel Heterozygous Mutation in Wilms Tumor 1 Gene in Patient with Mixed Gonadal Dysgenesis

      hrp0092p3-230
    • Falsely Elevated Serum Sex Steroid Hormones in a Girl with Premature Adrenarche

      hrp0092p3-231
    • NR5A1 Gene Mutation: Variable Phenotypes, New Variants, Different Outcomes

      hrp0092p3-232
    • Early Embryonic Testicular Regression Syndrome Presenting with Female External Genitalia

      hrp0092p3-233
    • Diagnostic Dilemma in a 46 XY Female

      hrp0092p3-234
    • Leydig Cell Hypoplasia in Three Siblings in the Same Family

      hrp0092p3-235
    • Klinefelter Syndrome Presenting with Learning Disabilities: Case Reports

      hrp0092p3-236
    • Gender Self-Identification and Intra-Family Relations in Children with Disorders of Sex Development

      hrp0092p3-237
    • Bilateral Testicular Atrophy and Normal Inhibin B level: A Paradoxal Clinical Finding For A Rare Biochemical Cause !

      hrp0092p3-238
    • Normosmic Hypogonadotropic Hypogonadism: An Intrafamiliar Case

      hrp0092p3-239
    • Testicular Regression Syndrome A Clinical and Pathologic Study of 4 Cases

      hrp0092p3-240
    • 46XY, DSD with Hemolytic Uremic Syndrome as the Primary Manifestation——Denys–Drash Syndrome Caused by WT1 Gene Mutation

      hrp0092p3-241
    • Clinical and Laboratory Characteristics of Patients with Different Variants of Gonadal Dysgenesis

      hrp0092p3-242
    • Etiologic Classification of 46, XY Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results

      hrp0092p3-243
    • Four-Year Experience of a New Referral Center for Gender Non-Conforming Children and Adolescents in North-East of Italy

      hrp0092p3-244
    • Ovarian Insufficiency: The Hidden Uterus

      hrp0092p3-245
    • An Adolescent Girl Presented with Hoarseness of Voice

      hrp0092p3-246
    • Turner's Syndrome Mosaicism 45X/47XXX with Iron Deficiency Anemia due to Menometrorrhagia

      hrp0092p3-247
    • Difficulties in Diagnosing Variable Disorders of Sexual Development

      hrp0092p3-248
  • Thyroid
  • • Association of Subclinical Hypothyroidism and Dyslipidemia in Children and Adolescents

      hrp0092p3-249
    • Evaluation of Clinical, Demographic Data and Treatment Results of Cases with Graves' Disease

      hrp0092p3-250
    • A Case of Graves Disease with Negative Thyrotropin Stimulating Antibodies in a Pediatric Patient with Type 1 Diabetes

      hrp0092p3-251
    • An Unusual Presentation of Hypothyridism: Van Wyk-Grumbach Syndrome

      hrp0092p3-252
    • Child Thyrotoxicosis Syndrome: Structure and Characteristics

      hrp0092p3-253
    • Encephalitis Associated with Autoimmune Thyroiditis: A Rare Cause of Encephalopathy In Children

      hrp0092p3-254
    • Association of BMI Z-Score and Subclinical Hypothyroidism in Children and Adolescents

      hrp0092p3-255
    • Pseudoprecocious Puberty in a Girl with Untreated Acquired Hypothyroidism

      hrp0092p3-256
    • Bilateral Hip Pain as First Symptomatic Expression of Severe Primary Hypothyroidism

      hrp0092p3-257
    • The Challenge to Treat Neonatal Autoimmune Hyperthyroidism in a Small Preterm

      hrp0092p3-258
    • Graves' Disease in a 3 Year-Old Patient with Agranulocytosis due to Methimazole

      hrp0092p3-259
    • Hashimoto's Thyroiditis in Children: Case Series Report of Three Patients

      hrp0092p3-260
    • Mutation of RET Gene Causes Multiple Endocrine Neoplasia Type 2B in an Adolescent: Report of One Case and Literature Review

      hrp0092p3-261
    • A 12 Year Old Boy with Multifocal Papillary Thyroid Carcinoma

      hrp0092p3-262
    • Papillary Thyroid Cancer in Children: Single Center Results

      hrp0092p3-263
    • Cardiac Tamponade Associated with Hypothyroidism in Rwandan Child

      hrp0092p3-264
  • Late Breaking Abstracts
  • • Plasma Asprosin Concentrations are Increased and Associated with Insulin Resistance in Children with Obesity

      hrp0092p3-265
    • A Novel Mutation of INSR Gene in a Child with Type A Insulin Resistance

      hrp0092p3-266
    • Indexes of Adiposity and Body Composition in the Prediction of Metabolic Syndrome in Obese Children and Adolescents: Which is the Best

      hrp0092p3-267
    • Clinical, Laboratory and Radiological Assessment of Obese and Non-Obese Girls Evaluated for Early Puberty

      hrp0092p3-268
    • IGSF1 Mutation: Treatment in the Absence of Symptoms?

      hrp0092p3-269
    • A Real World, Clinical Experience of Burosumab Therapy in a Cohort of Children with X-Linked Hypophosphataemia

      hrp0092p3-270
    • Psychosocial Wellbeing of Parents and Quality of Life of Children (Qol) with 46, XY Disorders of Sex Development (DSD) Attending The Endocrine Clinics at Lady Ridgeway Hospital (LRH) for Children

      hrp0092p3-271
    • The Effect of Aromatase Inhibitors on Treating Adolescent Boys with Short Stature: A Meta-Analysis of Randomized Controlled Trials

      hrp0092p3-272
    • Insulin Sensitivity as Homa at Start and End of HGH Treatment of Children with Congenital (C) Ighd and Mphd

      hrp0092p3-273
    • Role of Adiposity Indexes in the Risk of Ketoacidosis (DKA) in Children with Type 1 Diabetes (T1D) at Onset

      hrp0092p3-274
    • Serum Spexin is Correlated with Lipoprotein(a) and Androgens in Normal-Weight, Overweight and Obese Adolescent Females

      hrp0092p3-275
    • Exocrine Pancreatic Insufficiency and Vitamin K Deficiency Associated to Octreotide Therapy in Congenital Hyperinsulinism: An Under-Recognized Potential Adverse Effect

      hrp0092p3-276
    • The Role of Urine AVP in the Diagnostic Pathway of Polyuria and Polydipsia Syndrome

      hrp0092p3-277
    • New Mutation of Gnas in a 2 Year Old Oncological Patient

      hrp0092p3-278
    • Relation between Levels of Atymullerian Hormone and Inhibin B and Spontaneous Puberty in Patients with Turner Syndrome – Preliminary Results

      hrp0092p3-279
    • Short, but Daily and Controlled Physical Activity of Children with Obesity has a Positive Effect on The Irisin and Chemerin Levels

      hrp0092p3-280
    • New Autosomal Dominant Mutation in Glucokinase Gene Causing Congenital Hyperinsulinism Diagnosed in Adulthood

      hrp0092p3-281
    • Incidence and Neonatal Risk factors of Short Stature and Growth Hormone Treatment in Japanese Preterm Infants Born Small for Gestational Age

      hrp0092p3-282
    • Comparison of Densitometric Aspects during the Transition Period in Patients with Congenital and Acquired Pituitary Deficiency: First Argentine Experience

      hrp0092p3-283
    • Demographic, clinical and Biochemical Characteristics of Pediatric Obesity: Interim Analysis of a Larger Prospective Study

      hrp0092p3-284
    • Mental Health of Both Child and Parents Play a Larger Role in Health Related Quality of Life of Obese and Overweight Children

      hrp0092p3-285
    • Alterations in Ambulatory Blood Pressure in Adolescents with Obesity

      hrp0092p3-286
    • Should Wereviewclinical Criteria to Diagnose SHOX Gene Mutations?

      hrp0092p3-287
    • Circulating Chemerin may be Associated with Early Vascular Pathology in Obese Children without Overt Arterial Hypertension – Preliminary Results

      hrp0092p3-288
    • Quality of Life of Patients with Type 1 Diabetes

      hrp0092p3-289
    • Etiologies and Clinical Patterns of Hypopituitarism in Sudanese Children

      hrp0092p3-290
    • Rare Causes for Paediatric Virilizing Tumors

      hrp0092p3-291
    • GnRHa are Effective to Treat Short Stature Children with Normal Puberty: A Systematic Review and Meta-Analysis

      hrp0092p3-292
    • Clinical Evolution of a Patient with Isolated Growth Hormone Deficiency Type IA Treated with rIGF1 for 5 Years After The Development of GH-antibodies

      hrp0092p3-293
    • Beck Depression Inventory Scores for Children with Some Chronic Diseases (Type I Diabetes Mellitus, Sickle Cell Anaemia, and AIDS) in University of Port Harcourt Teaching Hospital

      hrp0092p3-294
    • A Novel Pathogenic Mutation of Vitamin-D-Dependent Rickets

      hrp0092p3-295
    • Neonatal Severe Hyperparathyroidism - Using Genetics to Determine Treatment

      hrp0092p3-296
    • Liver Transplantation in Saudi Homozygous Familial Hypercholesterolemia Patients

      hrp0092p3-297
    • Mitchell-Riley Syndrome, A Report of Novel Mutation in a Palestinian Family Resulting in Neonatal Diabetes

      hrp0092p3-298
    • Review of Neonatal Cortisol Evaluation between 2012-2018 in a Single Centre: Trends, Outcomes and Associations

      hrp0092p3-299
    • Height and Upper/Lower Body Ratio in Turner Syndrome Adolescents in Indonesia; Is There any Significant Difference Based on Karyotype?

      hrp0092p3-300
    • A Novel Heterozygous Mutation in The SLC5A2 Gene Causing Mild Failure to Thrive and Subclinical Hypoglycemia in a 2-year Old Girl

      hrp0092p3-301
    • Cognitive and Learning Performance of Children and Adolescents Cancer Survivors

      hrp0092p3-302
    • Hirsutism in Children: Pitfalls and Diagnostic Challenges

      hrp0092p3-303
    • Congenital Craniopharyngioma - A Rare Case of Congenital Hypopituitarism

      hrp0092p3-304
    • Combined Surgical and Medical Treatment in an Adolescent with Severe Gynecomastia Due to Excessive Estradiol Secretion: A Case Report

      hrp0092p3-305
    • Improvement of Metabolic Control in Children with Type1 Diabetes Using Continuous Glucose Monitoring Devices

      hrp0092p3-306
    • Autoimmune Thyroiditis in Beta Thalassemia Major after the Hematopoietic Stem Cell Transplantation - Case Report

      hrp0092p3-307
    • Grave's Disease: What Place in the Child's Hyperthyroidism?

      hrp0092p3-308
    • Vitamin D Status Among Children and Adolescents in an Egyptian Cohort: Can we Predict Vitamin D Deficiency?

      hrp0092p3-309
    • Case Report: Primary Hyperparathyroidism Presenting as a Brown Tumor of Mandible in an Adolescent Girl - An Unusual Presentation with Challenges and Outcome

      hrp0092p3-310
    • Serum Calcium, 25(OH) Vitamin D and Bone Alkaline Phosphatase in Children with Epilepsy Receiving Antiepileptic Drugs in University of Port Harcourt Teaching Hospital

      hrp0092p3-311
    • Emotional Status Instability and Body Mass Index as Predictive Markers for Dopamine System Dysfunction Evaluation in Pubertal Age Children

      hrp0092p3-312
    • A Case Report of Persistent Hyperinsulinemic Hypoglycemia of Infant

      hrp0092p3-313
    • Case Report: Hyperglicemic Iperosmolar State in a Obese Prepubertal Girl with Newly Diagnosis of Type 2 Diabetes

      hrp0092p3-314
    • Associations between Pituitary Abnormalities and Treatment Response in Children with Growth Hormone Deficiency. First Multicenter Study in Portugal

      hrp0092p3-315
    • Epidemiological and Socioeconomic CHANGES in the Child Population from Debut DM1 in this 21st Century

      hrp0092p3-316
    • Body Mass Index and Incident Type 1 Diabetes in Children from Lesser Poland Over an 11 Year Observation Period

      hrp0092p3-317
    • Novel Mutation in HNF4-Alpha Gene and Reclassification of Diabetes in a Family

      hrp0092p3-318
    • Systemic Lupus Erythematosus, Celiac and Hypothyroidism Complicating Type 1 Diabetes: A Rare Tetrad

      hrp0092p3-319
    • EpiPEG-PreMeb Study: Chemerina Plasmatic and Metabolic Syndrome Relation at SGA Childrens

      hrp0092p3-320
    • Hydrometrocolpos Due to Congenital Adrenal Hyperplasia – A Rare Cause of Bladder Outflow Tract Obstruction in a Female Child

      hrp0092p3-321
    • Bartter Syndrome Complicated with Growth Hormone Deficiency Due to a Suprasellar Arachnoid Cyst

      hrp0092p3-322
    • De Novo PPM1D Mutation in a Patient with Growth Hormone Deficiency: A Case Report

      hrp0092p3-323
    • Hypoglycemia in a Patient with Turner Syndrome and Kabuki Make-Up

      hrp0092p3-324
    • 45X/47XXX Mosaicism and Progressive Puberty

      hrp0092p3-325
    • Vitamin D and Type 1 Diabetes Mellitus in Children

      hrp0092p3-326
    • Severe Hypercalcaemia After Years on The Ketogenic Diet: A Novel Case Report

      hrp0092p3-327
    • Estrogen Production by Sertoli Cell Tumor in Unusual Case of Testicular Feminization Syndrome

      hrp0092p3-328
    • Dysphagia and Dyspnea by Lingual Thyroid Mass in a Young Child: What To Do?

      hrp0092p3-329
    • Van-Wyk Grumbach Syndrome Associated with Trisomy 21: A Case Report

      hrp0092p3-330
    • Fahr Syndrome in Young Boy with Hypoparathyroidism

      hrp0092p3-331
    • Thyroid Cancer in a Child with Graves's Disease

      hrp0092p3-332
    • Influence of Nocturnal Hypoglycemia on School Performance of Teens with DM Type1

      hrp0092p3-333