ePosters

HRP0092RFC1.1

Low Prevalence of Maternal Microchimerism in Japanese Children with Type 1 Diabetes
Direct

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HRP0092RFC1.3

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

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HRP0092RFC1.4

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

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HRP0092RFC1.5

Decreased Circulating Levels of MOTS-c in Individuals with Newly Diagnosed Type 1 Diabetes Children
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HRP0092RFC1.6

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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HRP0092RFC2.2

Does the Treatment with Recombinant Human Growth Hormone Improve Final Height in Patients Affected by X-Linked Hypophosphatemia?
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HRP0092RFC2.3

Growth Hormone Effects on Metacarpal Bone Geometry and Bone Age in Growth Hormone-Deficient Children
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HRP0092RFC2.4

Bone Mass and Fracture Prevalence in Childhood Brain Cancer Survivors 2, 5 or 7 Years After Off Therapy
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HRP0092RFC2.5

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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HRP0092RFC3.1

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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HRP0092RFC3.2

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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HRP0092RFC3.3

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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HRP0092RFC3.4

Peripheral Glucocorticoid Metabolim May Reflect Resolution of Inflammation in Kawasaki Disease
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HRP0092RFC3.5

Evaluation of Endothelial Function in Childhood Standard Risk Acute Lymphoblastic Leukemia Survivors: Role of Subclinical Markers and Identification of Preventable Factors
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HRP0092RFC3.6

Prevalence of Endocrine Complications in Duchenne Muscular Dystrophy
Direct

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HRP0092RFC4.2

Circulating Exosomal miRNAs in Children's Nonalcoholic Steatohepatitis and the Correlation with Serum Transaminase and Uric Acid
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HRP0092RFC4.3

Dysregulated Gene Expression Profile in Visceral Adipose Tissue of Juvenile Wistar Rats with Catch-Up Growth: Association with Fat Expansion and Metabolic Parameters
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HRP0092RFC4.4

The Novel Phosphatidylinositol-3-Kinase (PI3K) Inhibitor Alpelisib Effectively Inhibits Growth of PTEN Haploinsufficient Lipoma Cells
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HRP0092RFC4.5

GDF5 Increased White Adipose Tissue Thermogenesis Through p38 MAPK Signaling Pathway in Fatty Acid-binding Protein 4-GDF5 Transgenic Mice
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HRP0092RFC4.6

Appetite Suppressing Effects of Glucoregulatory Peptides Devoid of Nausea
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HRP0092RFC5.1

Hurthle Cell Carcinoma in Childhood: Retrospective Analysis of a Large Series
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HRP0092RFC5.2

Ultrasound Features of Multinodular Goiter in DICER1 Syndrome
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HRP0092RFC5.3

Experience of Thyroid Surgery in Children with Intraoperative Neuromonitoring
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HRP0092RFC5.4

Thyroid Dysfunction in Patients Following Thymus Transplantation in a Tertiary Centre: A 10-Year Experience
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HRP0092RFC5.5

A Novel Mutation in the Thyroglobulin Gene Leading to Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant
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HRP0092RFC6.1

EFTUD2 Gene Deficiency Disturbs Maturation of Osteoblast and Inhibits Chondrocyte Differentiation via Activated p53 Signaling
Direct

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HRP0092RFC6.3

Increased Burden of Common Risk Alleles in Children with a Significant Fracture History
Direct

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HRP0092RFC6.4

Targeted Molecular Genetic Diagnosis by Next Generation Sequence Analysis Method and Investigation of Responsible Candidate Genes in Patients with Osteogenesis Imperfecta
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HRP0092RFC6.6

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
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HRP0092RFC7.1

Accuracy of Glucose Sensor Estimate of HbA1c in Children with Type 1 Diabetes
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HRP0092RFC7.3

Osteopontin as an Early Urinary Marker of Diabetic Nephropathy in Adolescents with Type 1 Diabetes Mellitus
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HRP0092RFC7.4

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
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HRP0092RFC7.5

Dual Diagnosis of Type 1 Diabetes and ADHD
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HRP0092RFC7.6

Health-Related Quality of Life and Diabetes Control in Immigrant and Italian Children and Adolescents with Type 1 Diabetes and in their Parents
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HRP0092RFC8.1

Trade-Off Between Olfactory Bulb and Eyeball Volume in Precocious Puberty
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HRP0092RFC8.2

Investigation of Imprinting Alterations in MKRN3 and DLK1 in a Cohort of Girls with Central Precocious Puberty Through Specific DNA Methylation Analysis
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HRP0092RFC8.3

Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5'-UTR Region of the Imprinted MKRN3 Gene
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HRP0092RFC8.4

Evaluation of Puberty in Patients with Noonan Syndrome and Mutations in the RAS/MAPK Genes
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HRP0092RFC8.5

CHD7 Mutations in Patients with Anosmic or Normosmic Idiopathic Hypogonadotropic Hypogonadism
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HRP0092RFC8.6

Growth, Pubertal Course and Long-Term Outcome of 46,XY Boys Born with Atypical Genitalia and Low Birthweight
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HRP0092RFC9.1

Targeted Next-Generation Sequencing for Congenital Hypothyroidism with Positive Neonatal TSH Screening Results
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HRP0092RFC9.3

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
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HRP0092RFC9.4

Correlation Between Genotype and Phenotype Characteristics in Children with Congenital Hyperinsulinism (CHI) in a Specialist Centre
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HRP0092RFC9.5

Spectrum of Neuro-Developmental Disorders in Children with Congenital Hyperinsulinism Due to Activating Mutations in GLUD1
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HRP0092RFC10.1

Contemporary Surgical Approach in CAH 46XX  Results from the I-DSD/I-CAH Registries
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HRP0092RFC10.2

Cryptorchid Boys with Abrogated Mini-Puberty Display Differentially Expressed Genes Involved in Sudden Infant Death Syndrome
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HRP0092RFC10.3

Level of Uncertainty in Diagnostic Evaluation of Boys With XY Disorders of Sex Development (DSD)
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HRP0092RFC10.4

qPCR Screening for Xp21.2 Copy Number Variations in Patients with Elusive Aetiology of 46,XY DSD
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HRP0092RFC10.5

Variants in NWD1 Gene Leading to Different Degrees of Gonadal Dysgenesis
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HRP0092RFC10.6

A Mutation in the Nucleoporin-107 Gene Causes Aberrant Dpp/BMP Signaling and XX Gonadal Dysgenesis
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HRP0092RFC11.1

National United Kingdom Evidence- and Consensus-Based Guidelines for the Investigation, Treatment and Long-Term Follow-Up of Paediatric Craniopharyngioma
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HRP0092RFC11.2

Prevalence and Predicting Factors of Endocrine Dysfunction in Children with NF1 and Optic Gliomas
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HRP0092RFC11.3

Polycystic Ovarian Syndrome in Adolescents: Utilising Discovery Proteomics and the Search for to Identify Novel Non-Invasive Biomarkers
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HRP0092RFC11.4

Increased Adrenal and Testicular Androgen Concentrations Before Puberty and in Early Puberty Correlate to Adult Height Outcomes in Males with Silver-Russell Syndrome
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HRP0092RFC11.5

IGF-1 Serum Concentrations and Growth in Children with Congenital Leptin Deficiency (CLD) Before and After Replacement Therapy with Metreleptin
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HRP0092RFC12.1

Karyotyping of Oocytes, Granulosa Cells and Stromal Cells in the Ovarian Tissue from Patients with Turner Syndrome: A Pilot Study
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HRP0092RFC12.3

Imprinting Defects and Copy Number Variations in Short Children Born Small for Gestational Age
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HRP0092RFC12.5

Cognitive and Neuroradiological Assessments in Silver Russell Patients
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HRP0092RFC12.6

Exploring the Usefullness of a New Type of Pubertal Heigh Reference Based on Growth Aligned or Onset of Pubertal Growth
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HRP0092RFC13.1

Children and Adolescents in the United States with Congenital Adrenal Hyperplasia are not at Increased Risk for Attention-Deficit/Hyperactivity Disorder
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HRP0092RFC13.2

Development of Novel Non-Invasive Strategies for Monitoring of Treatment Control in Patients with Congenital Adrenal Hyperplasia
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HRP0092RFC13.4

Loss-Of-Function NNT Mutations Impair Antioxidants Mechanisms and Decreases Cortisol Secretion in Patients with Famililar Glucocorticoid Deficieny
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HRP0092RFC13.5

Genetics of Familial Glucocorticoid Deficiency Over the Decades: Phenotypic Variability and Associated Features
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HRP0092RFC13.6

Inhibitory Effects of Curcuminoids on the Enzymes from the Steroidogenic Pathway
Direct

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HRP0092RFC14.1

PAPP-A2 Deficiency Results in Sex-Dependent Modifications in Hypothalamic Regulation of Energy Homeostasis
Direct

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HRP0092RFC14.2

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
Direct

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HRP0092RFC14.3

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
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HRP0092RFC14.4

GHR Transcript Heterogeneity May Explain the Phenotypic Variability in Patients with Homozygous GHR Pseudoexon (6ψ) Mutation
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HRP0092RFC14.5

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)
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HRP0092RFC14.6

Growth Hormone Deficiency (GHD): Assessing Burden of Disease in Children and Adolescents: The Growth Hormone Deficiency  Child Impact Measure (GHD-CIM)
Direct

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HRP0092RFC15.2

BMP4 Mutations as a Novel Cause of Normosmic Hypogonadotropic Hypogonadism
Direct

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HRP0092RFC15.3

Metformin Treatment Affects ACTH Receptor Activation and Downstream Signaling: A Potential Treatment for ACTH Excess Disorders and Management of Hyperandrogenic States
Direct

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HRP0092RFC15.4

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

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HRP0092RFC15.6

Absence of Puberty and Estrogen Resistance by Estrogen Alpha Receptor Inactivation in Two Sisters: A Mutation for Variable Phenotypic Severity
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HRP0092T1

Circulating miR-451a: A Biomarker to Guide Diagnosis and Treatment of Polycystic Ovary Syndrome in Adolescent Girls
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HRP0092T2

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

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HRP0092T3

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

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HRP0092T4

Use of Stored Serum in the Study of Time Trends and Geographical Differences in Exposure of Pregnant Women to Phthalates
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HRP0092T6

Obesity in Pediatric Age: The Analysis of Genomic Rearrangements
Direct

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HRP0092T7

Establishing of a Novel NGS Tool for the Diagnosis of X-linked Hypophosphatemia (XLH)
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HRP0092T8

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

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HRP0092T9

Empagliflozin and GABA Improve β-Cell Mass and Glucose Tolerance in New-Onset Type 1 Diabetes
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HRP0092T10

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

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HRP0092T11

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

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HRP0092T12

The First Description of Large Pathogenic Deletion in ACAN Gene and Additional Cases with Novel Pathogenic ACAN Variants
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HRP0092T13

Results from the Implementation of a 2 Year Growth Awareness and Growth Disorders Screening Campaign (GrowInform)
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HRP0092T14

The Effect of Endocine Disrupting Chemicals to Precocious Puberty in Children with Exposure History of 'Slim'
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HRP0092T15

Intestinal Microbiota Development Differs Between Pubertal Boys and Girls
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HRP0092T16

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

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HRP0092T17

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

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HRP0092T18

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

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HRP0092T19

Urinary Gonadotrophins in Girls with Turner Syndrome
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HRP0092T20

Molecular and Phenotypic Spectrum of Noonan Syndrome in Chinese Patients
Direct

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HRP0092P1-1

Could a Glucocorticoid Receptor Polymorphism be Protective against Hypothalamic-Pituitary-Adrenal Axis Suppression in Asthmatic Children on Corticosteroids?
Direct

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HRP0092P1-2

Software-assisted Analysis of the Urinary Steroid Metabolom in Treated Children with Classic Congenital Adrenal Hyperplasia
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HRP0092P1-3

Simplifying the Interpretation of Steroid Metabolome Data by a Machine-Learning Approach
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HRP0092P1-4

The Steroidal Milieu in Amniotic Fluid of Mid-Gestation: A Targeted GC-MS Metabolomics Study
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HRP0092P1-5

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
Direct

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HRP0092P1-6

Health status of children with Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency in the United Kingdom: results of a multi-centre cohort study
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HRP0092P1-8

Follow-up and Prevalence of Precocious Puberty in Children with Classical Congenital Adrenal Hyperplasia diagnosed by Neonatal Screening
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HRP0092P1-9

A Simulation-based Intervention Teaching Illness Management Skills to Caregivers of Children with Adrenal Insufficiency: a Randomised Controlled Study
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HRP0092P1-10

Global Practice of Glucocorticoid and Mineralocorticoid Treatment in Children and Adults with Congenital Adrenal Hyperplasia  Insights from the I-CAH Registry
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HRP0092P1-11

Assessment of the Adrenal Function in Children with Acute Lymphoblastic Leukemia Before and After Induction Therapy with Corticosteroids
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HRP0092P1-12

Trientine Treatment Mimicking Severe Hyperandrogenism
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HRP0092P1-13

Cytokines and the Impairment of Puberty
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HRP0092P1-14

Refractory Hypercalcemia After Denosumab Treatment in Pediatric Age: A Case Report
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HRP0092P1-15

The Overweight and Obesity Decrease the Growth Potential in Mexican Children and Adolescents
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HRP0092P1-16

Normocalcemic Hyperparathyroidism in Children
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HRP0092P1-17

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
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HRP0092P1-18

Nephrocalcinosis in Children with X-Linked Hypophosphatemia: Prevalence and Risks Factors
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HRP0092P1-20

Long-term Teriparatide (rhPTH) Treatment in Children with Syndromic Hypoparathyroidism
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HRP0092P1-21

Dual X-ray Absorptiometry in Children With Hypophosphatasia Treated with Asfotase Alfa: A Pooled Post Hoc Analysis
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HRP0092P1-22

Differences in Bone Strength and Cortical Bone Parameters in Young Swedish Women with Type 1 Diabetes
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HRP0092P1-23

Increased Prevalence of Overweight and Obesity and its Clinical Predictors in Children Affected by X-Linked Hypophosphatemia
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HRP0092P1-24

Novel Homozygous LRP5 Mutations in Patients with Osteoporosis-Pseudoglioma Syndrome
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HRP0092P1-25

Pathogenicity of GCK Gene Mutation c.364C>G (p.Leu122Val)
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HRP0092P1-26

Myocardial Function in Asymptomatic Children with Type 1 Diabetes
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HRP0092P1-27

A Case of Neonatal Diabetes with Hyperferritinemia: A Distal PTF1A Enhancer Mutation
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HRP0092P1-28

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

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HRP0092P1-29

What Hypoglycemia Does to the Heart: Impact of Nocturnal Hypoglycemia on Cardiac Repolarization in Diabetic Children
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HRP0092P1-30

Effects of Glypican-4 Protein on INS1E Cell Viability and Insulin Signalling
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HRP0092P1-32

Heterozygous RFX6 Mutation as a Cause of Diabetes Mellitus in a Multigenerational Family
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HRP0092P1-34

Serum Dipeptidyl peptidase-4 Activity and its Relation to Insulin Resistance in Type 1 Diabetic Adolescents
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HRP0092P1-35

The Impact of CGM Availability: Real World Data From a Population Based Clinic
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HRP0092P1-36

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
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HRP0092P1-37

Association of Maternal Depressive Symptoms with Worse Metabolic Control in Adolescents with Type 1 Diabetes
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HRP0092P1-38

The Factors Associated with High Levels of HbA1C in Children and Young People with Type 1 Diabetes Mellitus
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HRP0092P1-39

Differences Between Short- and Long-term Outcomes of Laparoscopic Sleeve Gastrectomy in Adolescence
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HRP0092P1-41

Growth Arrest-Specific 6 (Gas6) Protein is Associated with Adiposity and Metabolic Syndrome in Obese Children and Adolescents
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HRP0092P1-43

Association of Biomarkers of Endothelial Dysfunction with MicroRNAs Levels in Overweight and Obese Adolescentes
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HRP0092P1-45

Non-Alcoholic Fatty Liver Disease and eGFR Levels could be Linked by the PNPLA3 I148M Polymorphism in Obese Children
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HRP0092P1-48

Waist Circumference Triglyceride Index is Useful to Predict Non-alcoholic Fatty Liver Disease in Childhood Obesity
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HRP0092P1-49

Gut Microbiome of North-American Children with and without Prader-Willi Syndrome (PWS)
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HRP0092P1-51

Pathogenic Mutations and Variants in KSR2 in a Cohort of Obese Children
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HRP0092P1-52

Effect of Feeding Mode on Longitudinal Body Composition in Early Life
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HRP0092P1-53

Age of Obesity Onset could be the First Indicator of Future Metabolic Complications  Preliminary Data of Prospective Multicenter Study
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HRP0092P1-54

Augmented Fibroblast Growth Factor 21 Serum Levels in Metabolic Disorders and Association With Endothelial Function in Childhood
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HRP0092P1-55

A Novel Recurrent Heterozygous Plin1 Mutation in Three Russian Patients with Partial Lipodystrophy, Dyslipidemia and Insulin Resistance
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HRP0092P1-56

Carotid Intima-Media Thickness Relates Rather to Epicardial and Perirenal Fat than Total Body Adiposity in Apparently Healthy Children
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HRP0092P1-57

Put Your Money Where Your Mouth is: Preliminary Evidence that Oral Microbiota Diversity may Shape Later Cardiometabolic Health in Children
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HRP0092P1-58

A Case-Control Study of Exposure to Bisphenol-a and Phthalates in Obese Children
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HRP0092P1-59

Growth Patterns in Non-syndromic Childhood Overweight: Comparing Children with Early of Late Onset Weight Gain
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HRP0092P1-63

Altered Gut Microbiota in Obese Children: Sex-associated Signature
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HRP0092P1-64

Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome
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HRP0092P1-65

Congenital Hyperinsulinism Due to Pancreatic Mosaicism for Paternal Uniparental Disomy of all Chromosome 11, with the Additional Finding of Pancreatic Mosaicism for Trisomy 12
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HRP0092P1-66

Diagnostical Approach to Adrenal Failure in Symptomatical Preterm Infants  is Saliva Derived Free Cortisol the Solution?
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HRP0092P1-67

Screening of Congenital Hypothyroidism using Umbilical Cord Blood in a Maternity Hospital
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HRP0092P1-70

Congenital Hypothyroidism  Precise Diagnosis with Dual Imaging
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HRP0092P1-71

Clinical, Biochemical and Echocardiographic Evaluation of Patients with Congenital Rickets Due to Maternal Vitamin D Deficiency
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HRP0092P1-72

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
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HRP0092P1-73

Influence of Birth Parameters on Growth Response and Metabolic Effects of Growth Hormone (GH) Therapy in GH-deficient Children and Adolescents
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HRP0092P1-74

Recombinant GH Treatment in Child with Pseudopseudohypoparathyroidism Associated with Growth Hormone Deficiency
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HRP0092P1-75

Impact of -202 IGFBP-3 Promoter Polymorphism on Growth Responses in Korean Children with Idiopathic Short Stature
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HRP0092P1-76

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)
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HRP0092P1-77

Severe IGF-I Deficiency in Children with Normal Growth Hormone (GH) Secretion and Excluded GH Insensitivity  is it Really Idiopathic Short Stature?
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HRP0092P1-79

The experience of Pain in Children with Growth Hormone Deficiency and Psychosocial Correlates: Preliminary Data from a Longitudinal Prospective Study
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HRP0092P1-80

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)
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HRP0092P1-82

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)
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HRP0092P1-83

Identification of Novel Recessive IGFALS Mutations and INSR Variant in an Obese Korean Boy
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HRP0092P1-84

Development of a Parent Experience Measure for Parents of Children with Achondroplasia
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HRP0092P1-85

Bone Mineral Density is Normal in Prepubertal Patients with Turner Syndrome when Corrected by Height/age
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HRP0092P1-86

Extreme Short Stature and Poor Pubertal Growth: When FBN1 is the Culprit
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HRP0092P1-88

Etiology of Severe Short Stature: Single Center Experience
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HRP0092P1-89

Clinical Outcomes in Primary Empty Sella (ES) Syndrome in Childhood-Onset Growth Hormone Deficiency: Data from KIGS (Pfizer International Growth Database)
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HRP0092P1-91

Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Panhypopituitarism Due to a Novel Heterozygous IVS11-2AC(c.1957-2AC) Mutation in GLI2 Gene
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HRP0092P1-92

A Rare Case of Pseudoisodicentric X Chromosome in a Patient with Primary Amenorrhoea
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HRP0092P1-93

Persisting Embryonal Infundibular Recess in a Patient with Morning Glory Syndrome and Multiple Pituitary Deficiencies
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HRP0092P1-94

Familial Occurrence of Turner Syndrome in two Tunisian Families
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HRP0092P1-95

The role of Physical Activity on Postural Stability and Fitness Characteristics in Pediatric Patients with GH Deficiency
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HRP0092P1-96

Assessment of Subjective and Objective Compliance to Growth Hormone Therapy of Children with Growth Hormone Deficiency
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HRP0092P1-97

Familial Neurohypophyseal Diabetes Insipidus and 2 Novel Vasopressin Gene Mutations in 13 Italian Kindreds.
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HRP0092P1-98

Final Height in Oncological Growth Hormone Deficient (GHD) Children After Growth Hormone (GH) Therapy
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HRP0092P1-99

Eating Behavior and Oxytocin in Childhood-onset Craniopharyngioma Patients: An Exploratory Study
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HRP0092P1-100

RNPC3 Mutations Associate Prolactin Deficiency and Ovarian Insufficiency, Expanding the Phenotype Beyond Isolated Growth Hormone Deficiency Type V (MIM#618860)
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HRP0092P1-101

Identification of Novel Mutations in FGFR1 and Functional Characteristics in Patients with Isolated Gonadotropin-Releasing Hormone Deficiency
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HRP0092P1-102

Clinical Presentation, Management, and the Outcomes of Pituitary Adenomas in Children
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HRP0092P1-103

A Case of Panhipopituitarism with SOX3 Gene Deletion
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HRP0092P1-104

Interesting Genotype-Phenotype Differences in Siblings with Familial Hypopituitarism and Pituitary Hypoplasia
Direct

Abstract PDF
HRP0092P1-105

Familial Central Precocious Puberty Caused by a Novel MKRN3 Mutation
Direct

Abstract PDF
HRP0092P1-106

Management and Treatment Outcome of Craniopharyngiomas in Young Children Before 4 Years of Age in Italy: Multicentre Collection of 16 Cases
Direct

Abstract PDF
HRP0092P1-109

A NCOA5 Gene Variant in A Pedigree With Maternally Inherited Precocious Puberty
Direct

Abstract PDF
HRP0092P1-110

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

Abstract PDF
HRP0092P1-111

PROKR2 in Girls with Idiopathic Central Precocious Puberty
Direct

Abstract PDF
HRP0092P1-114

Obesity in Boys is Not Associated with Delayed Pubertal Onset
Direct

Abstract PDF
HRP0092P1-115

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

Abstract PDF
HRP0092P1-116

How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty
Direct

Abstract PDF
HRP0092P1-117

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

Abstract PDF
HRP0092P1-118

Whole Exome Sequencing (WES) Reveals Oligogenic Gene Mutations in a Case of Combined Pituitary Hormone Deficiency (CPHD)
Direct

Abstract PDF
HRP0092P1-119

Menarche and its Relation to the Pubertal Growth Spurt
Direct

Abstract PDF
HRP0092P1-120

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

Abstract PDF
HRP0092P1-121

Lower Urinary Tract Dysfunction and Infection in Girls with Disorders of Sex Development and Urogenital Sinus
Direct

Abstract PDF
HRP0092P1-123

Does the Internet Provide Accurate and Valid Health Information Regarding Disorders of Sex Development?
Direct

Abstract PDF
HRP0092P1-124

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

Abstract PDF
HRP0092P1-125

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

Abstract PDF
HRP0092P1-126

Longitudinal Changes in External Masculinisation Scores in Boys with XY Disorder of Sex Development (DSD)
Direct

Abstract PDF
HRP0092P1-127

Mutations in CBX2 Associated with Gonadal Anomalies in 46,XY and 46,XX Individuals
Direct

Abstract PDF
HRP0092P1-128

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

Abstract PDF
HRP0092P1-129

Molecular Diagnosis of Patients with 46,XY Differences in Sex Development in A Single Tertiary Center
Direct

Abstract PDF
HRP0092P1-131

Is there the Relationship Between Anxiety and Depression Level and Clinical Presentation of Polycystic Ovary Syndrome in Adolescent Girls?
Direct

Abstract PDF
HRP0092P1-132

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
Direct

Abstract PDF
HRP0092P1-135

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

Abstract PDF
HRP0092P1-136

Serum Estradiol is Associated with Inhibin B in Healthy 1-6 Years Old Girls
Direct

Abstract PDF
HRP0092P1-137

Brain MRI Findings in Girls with Central Precocious Puberty in Taiwan: One Medical Center Experience
Direct

Abstract PDF
HRP0092P1-138

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

Abstract PDF
HRP0092P1-139

Gonadal Function of Female Patients with Noonan Syndrome
Direct

Abstract PDF
HRP0092P1-140

Methylation Status of X Inactivation-Escape Genes in Controls and Females with X Chromosome Rearrangements
Direct

Abstract PDF
HRP0092P1-141

Diagnostic Value of Anti-Mullerian Hormone Level in Adolescent Females with Polycystic Ovary Syndrome
Direct

Abstract PDF
HRP0092P1-142

Disorders of Sex Development (DSD): Inconsistencies Between Clinical Features and Peripheral Blood Cultured Karyotypes
Direct

Abstract PDF
HRP0092P1-143

Biotine interference in a patient with non-clinic high thyroid hormone levels
Direct

Abstract PDF
HRP0092P1-145

The Investigation of Genetic Etiology in Familial Cases with Congenital Hypothyroidism
Direct

Abstract PDF
HRP0092P1-146

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

Abstract PDF
HRP0092P1-147

Intrathyroidal Ectopia of Thymus in Children: Frequency, Ultrasound, Evolution
Direct

Abstract PDF
HRP0092P1-148

Activating Mutation M453V in Receptor TSHR as a Cause Familial Hyperthyroidism
Direct

Abstract PDF
HRP0092P1-149

Central Hypothyreoidism with Pituitary Enlargement and No Gene Alterations
Direct

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HRP0092P1-152

Thyroid Function Following Hemithyroidectomy in a Pediatric Cohort
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Abstract PDF
HRP0092P1-153

Homozygous c.2422delT hTPO Mutation in Three Patients with Congenital Hypothyroidism Followed Over 20 Years
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HRP0092P1-154

Association of Hashimoto's Thyroiditis with Antistreptolysin O titer
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Abstract PDF
HRP0092P1-156

Prospective, Open-Label, Long-Term Follow-Up of Neonates and Young Children with Adrenal Insufficiency Treated with Hydrocortisone Granules
Direct

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HRP0092P1-157

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
Direct

Abstract PDF
HRP0092P1-159

Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency
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Abstract PDF
HRP0092P1-160

Serum fetuin-A and insulin levels in classic congenital adrenal hyperplasia
Direct

Abstract PDF
HRP0092P1-161

Perioperative Control of Blood Pressure in a Child with Paraganglioma Using Esmolol
Direct

Abstract PDF
HRP0092P1-162

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

Abstract PDF
HRP0092P1-164

The Urinary Steroid Signature of Premature Adrenarche
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HRP0092P1-165

How the Level of Antibodies Against 21-Hydroxylase Changes with Time in Patients with Addison's Disease
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Abstract PDF
HRP0092P1-166

Cortisol levels in glucagon stimulation tests in children evaluating for short stature: clinical and laboratorial correlations
Direct

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HRP0092P1-167

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

Abstract PDF
HRP0092P1-168

Genotype-Phenotype Characteristics in Four Families of Type II Collagenopathy in Our Hospital
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Abstract PDF
HRP0092P1-170

Efficacy and Safety of Denosumab Treatment in a Boy with Cherubism
Direct

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HRP0092P1-171

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

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HRP0092P1-173

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

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HRP0092P1-174

The Optimal Dosage of Vitamin D Supplement for Vitamin D deficiency in Korean Children and Adolescents
Direct

Abstract PDF
HRP0092P1-175

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees
Direct

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HRP0092P1-176

Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA
Direct

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HRP0092P1-177

Severe Hypocalcaemia in Propionic Acidaemia caused by Parathyroid Hormone Resistance and treated with Alfacalcidol
Direct

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HRP0092P1-178

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
Direct

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HRP0092P1-179

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
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HRP0092P1-180

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
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HRP0092P1-181

A Case of Prohormone Convertase Deficiency Diagnosed with Type 2 Diabetes Mellitus
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HRP0092P1-182

The Influence of Excess Iron on Pancreatic Beta Cells
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HRP0092P1-183

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

Abstract PDF
HRP0092P1-184

A Case with Monogenic Diabetes Caused by RFX6 Mutation in a 14-Year-Old-Girl
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HRP0092P1-185

Endothelial and Heart Dysfunction in Children and Adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0092P1-188

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
Direct

Abstract PDF
HRP0092P1-189

A Novel SLC2A2 Mutation Implicated in Fanconi Bickel Syndrome and Dysglycemia
Direct

Abstract PDF
HRP0092P1-191

Effect of Probiotics Intake on Obese Children
Direct

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HRP0092P1-192

Changes in Objectively Measured Sleep Quality After an Integral Intervention in Patients with Abdominal Obesity
Direct

Abstract PDF
HRP0092P1-193

Circulating Insulin-Like Growth Factor-I Independently Predicts Blood Pressure in Apparently Healthy Children
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Abstract PDF
HRP0092P1-195

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

Abstract PDF
HRP0092P1-197

You are What You Eat: Preliminary Evidence of Associations Between Dietary Habits and Oral Microbiota Composition in Early Childhood
Direct

Abstract PDF
HRP0092P1-198

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

Abstract PDF
HRP0092P1-199

Non-Alcoholic Fatty Liver Youth with Obesity
Direct

Abstract PDF
HRP0092P1-201

Serum Kisspeptin in Obese Children and its Relation to Glucose Metabolism
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HRP0092P1-202

Visceral Adiposity Index as a Marker of Metabolic Risk in Survivors of Paediatric Hematopoietic Stem Cell Transplantation After Chemotherapy-Only Conditioning
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HRP0092P1-203

Serum Nonylphenol and Obesity in Children and Adolescents
Direct

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HRP0092P1-204

Risk Factors for Brain Injury After Transient or Persistent Hyperinsulinemic Hypoglycemia in Neonates
Direct

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HRP0092P1-205

Central Hypoventilation Syndrome and Hyperinsulinameic Hypoglycaemia
Direct

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HRP0092P1-206

Unusual Congenital Hyperinsulinism Case in a Patient with a Pathogenic GCK Mutation
Direct

Abstract PDF
HRP0092P1-207

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

Abstract PDF
HRP0092P1-209

Urogenital Abnormalities in Children Conceived by Assisted Reproductive Technologies
Direct

Abstract PDF
HRP0092P1-210

Subcutaneous Fat Necrosis of the Newborn: A Systematic Review of the Literature
Direct

Abstract PDF
HRP0092P1-211

Characteristics of Children with Kabuki Syndrome and Hyperinsulinemic Hypoglycemia
Direct

Abstract PDF
HRP0092P1-213

Determinants of Final Height in Patients Born Small for Gestational Age Treated with Recombinant Growth Hormone
Direct

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HRP0092P1-215

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
Direct

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HRP0092P1-218

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

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HRP0092P1-220

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

Abstract PDF
HRP0092P1-221

Individual Patterns of Objectively Measured Adherence to Growth Hormone Treatment and its Effect on Growth in Prepubertal Children with Growth Hormone Deficiency
Direct

Abstract PDF
HRP0092P1-222

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

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HRP0092P1-223

Tall Stature and Macrodactyly of the Great Toes Due to a Novel Mutation in the Natriuretic Peptide Receptor-2 Gene
Direct

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HRP0092P1-225

The Phenotypic Spectrum of Kabuki Syndrome in Patients of Chinese Descent
Direct

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HRP0092P1-226

Response to Growth Hormone in Very Young Children (® International Outcome Study and ANSWER Program
Direct

Abstract PDF
HRP0092P1-228

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

Abstract PDF
HRP0092P1-229

"Endocrine Evaluation of 29 Cornelia de Lange Syndrome Patients (CdLS) Patients"
Direct

Abstract PDF
HRP0092P1-231

Height and Weight Dynamics in Preschool Boys with Constitutional Delay of Growth and Puberty
Direct

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HRP0092P1-232

Two Chinese Children with FBN1-Related Acromelic Dysplasia
Direct

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HRP0092P1-233

Growth Patterns Over Two Years After Birth According to the Birth Weight and Length Percentile in Children Born Preterm
Direct

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HRP0092P1-234

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

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HRP0092P1-235

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

Abstract PDF
HRP0092P1-236

Serum Endocan Levels as a Marker of Endothelial Dysfunction in Turner Syndrome and Correlation with Cardiac Findings
Direct

Abstract PDF
HRP0092P1-237

The Effects of Fetal Electromagnetic Field Exposure on Expression of Anxiety Behavior and Associated Genes in Adolescent Period
Direct

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HRP0092P1-238

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

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HRP0092P1-239

Unusual Presentation of Autoimmune Polyglandular Syndrome Type 1 (aps1)
Direct

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HRP0092P1-240

Association of Tuberous Sclerosis Complex (TSC) and Insulinoma in a Pediatric Patient
Direct

Abstract PDF
HRP0092P1-241

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

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HRP0092P1-242

Basal Metabolic Rate in Polycystic Ovary Syndrome: A Meta-Analysis
Direct

Abstract PDF
HRP0092P1-243

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

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HRP0092P1-244

Two Different Endocrine Cancer, One Disease; DICER-1 Mutation
Direct

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HRP0092P1-245

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

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HRP0092P1-246

Knowledge of the Natural History of Paediatric MEN1 is Required to Inform Decision Making for Predictive Testing in Childhood
Direct

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HRP0092P1-247

One AIRE Gene Mutation and Two Different Clinical Manifestations in a Couple of Brothers
Direct

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HRP0092P1-248

A Novel AIRE Gene Mutation in Two Siblings Revealing Different Phenotypes of Autoimmune Polyendocrine Syndrome Type 1
Direct

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HRP0092P1-249

Use of Desmopressin for Bilateral Inferior Petrosal Sinus Sampling (BIPSS) in Pediatric Patients with Cushing Disease (CD)
Direct

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HRP0092P1-250

Correlation Between Pubertal Growth and Testicular Volume in Boys a Longitudinal Study
Direct

Abstract PDF
HRP0092P1-251

Central Diabetes Insipidus in Children: Role of GH Antibodies
Direct

Abstract PDF
HRP0092P1-252

Brain Malformations and Sellar Spine as Possible Causes of Central Precocious Puberty in a Large Monocentric Study
Direct

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HRP0092P1-253

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

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HRP0092P1-254

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

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HRP0092P1-255

Effects of 5-Hydroxymethylfurfural on Pubertal Development of Wistar Rats
Direct

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HRP0092P1-256

Kisspeptin Levels is a New Diagnostic Approach of Hypogonadotropic Hypogonadism in Boys
Direct

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HRP0092P1-257

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

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HRP0092P1-258

Novel Pubertal References for Girls Using Ultrasound to Stage Breast Development. The Bergen Growth Study 2
Direct

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HRP0092P1-259

Disruption of Hypothalamic Regulation of Appetite Associated with Proton Beam Therapy
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HRP0092P1-260

A Case-Control Study of Exposure to Bisphenol-A and Phthalates in Girls with Early Onset of Puberty
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HRP0092P1-261

Long-Term Urological and Psychosexual Outcome of Men Born with Hypospadias
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HRP0092P1-262

Long-Term Outcome in Leydig Cell Hypoplasia
Direct

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HRP0092P1-263

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

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HRP0092P1-265

Dynamics in Blood Pressure After Pubertal Suppression with GnRH Analogs Followed by Testosterone Treatment in Male Adolescents
Direct

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HRP0092P1-266

A Nationwide Study of the Prevalence & Initial Management of Atypical Genitalia & Delayed Sex Assignment in the Newborn
Direct

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HRP0092P1-267

Endocrine Profiling and Association with Ultrasound Measured Testicular Volume and Biometrics in a Cohort of Norwegian Boys
Direct

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HRP0092P1-268

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

Abstract PDF
HRP0092P1-269

The Impact of Klinefelter Syndrome on Quality of Life  a Multicentre Study
Direct

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HRP0092P1-270

Large Spectrum of DSD Phenotype Caused by Pathogenic Variants in Wilms Tumor Suppressor Gene 1
Direct

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HRP0092P1-271

Endocrine and Reproductive Outcome of Men Born with Various Degrees of Hypospadias
Direct

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HRP0092P1-272

Age at Menarche Over the Last Decades and Inter-Regional Variability in Northern Spain
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HRP0092P1-273

Hypergonadotropic Hypogonadism in 46, XX Adolescents Without Gonadotoxic Therapy: Clinical Features and Molecular Etiologies
Direct

Abstract PDF
HRP0092P1-274

Quality of Life in Chilean Transgender Children, Adolescents, and Their Parents
Direct

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HRP0092P1-275

Long-Term Outcome of Testicular Function in Nonclassic Lipoid Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0092P1-279

Gender Mender, or Defender: Understanding Decision Making in Aotearoa/New Zealand for People Born with a Variation in Sex Characteristics
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HRP0092P1-281

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
Direct

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HRP0092P1-282

Characteristics of 311 Children with Early Onset Pubertal Signs. Descriptive Study
Direct

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HRP0092P1-283

Children with Hashimoto's Thyroiditis have Increased Intestinal Permeability: Results of a Pilot Study
Direct

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HRP0092P1-284

Different Endocrine Affects in DICER-1 Syndrome
Direct

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HRP0092P1-285

Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases
Direct

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HRP0092P1-286

Identification of a THRA Mutation in a 2yr Old Child with Clinical Features of Hypothyroidism and Multisystem Involvement
Direct

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HRP0092P1-287

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
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HRP0092P1-288

Outcomes of Persistent Hyperthyrotropinaemia in Well Term Infants
Direct

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HRP0092P1-289

Thyroid Peroxidase Antibodies in Children with HLA-Conferred Susceptibility to Type 1 Diabetes
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HRP0092P1-290

Prediction of Permanent and Transient Congenital Hypothyroidism Based on Levothyroxine Dosages in Long-Term Follow-Up Patients: A Multicenter Retrospective Study in Japan
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HRP0092P1-291

An Incidental Finding of Thyroid Hormone Resistance Due to a De Novo Mutation in the THRB Gene
Direct

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HRP0092P1-292

Outcome of Congenital Hypothyroidism in Algeria: The Urgent Need to Implement a National Newborn Screening Program
Direct

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HRP0092P1-296

Three Novel Mutations of the StAR Gene in Five Algerian Patients Presenting with Classical and Non-Classical Lipoid Adrenal Hyperplasia
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HRP0092P1-297

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

Abstract PDF
HRP0092P1-298

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

Abstract PDF
HRP0092P1-299

Medical Identification Jewellery Use in Children and Young Adults with Adrenal Insufficiency
Direct

Abstract PDF
HRP0092P1-300

Growth Trajectory and Final Height in Children with Non Classical Congenital Adrenal Hyperplasia
Direct

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HRP0092P1-301

Height in Infants Aged 1 Year with Classic Congenital Adrenal Hyperplasia is Related to their Urinary Steroid Metabolome
Direct

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HRP0092P1-305

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

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HRP0092P1-306

Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience
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HRP0092P1-307

"CAH-X" Due to Homozygous Deletions of CYP21A2 and TNXB Exon 35 in a Newborn from the 17 OHP Screening
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HRP0092P1-308

ABCC8 MODY in an Obese Adolescent Misdiagnosed with Type 2 Diabetes
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HRP0092P1-309

Level of Glycemic Control in Pediatric Patients with Type 1 Diabetes in Bern: A Cross-Sectional Study
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HRP0092P1-310

Preliminary Results of Public Health Prevention Program for Diabetic Ketoacidosis in Children and Adolescent
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HRP0092P1-311

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

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HRP0092P1-313

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

Abstract PDF
HRP0092P1-316

An Evaluation of the Accuracy of a Flash Glucose Monitoring System in Children with Diabetes in Comparison with Venous Blood Glucose
Direct

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HRP0092P1-317

Unexplained Neonatal Deaths Among Kurdish Consanguineous Families: Importance of Recognizing Congenital Hyperinsulinism and Testing for KATP Channel Gene Variants
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HRP0092P1-319

Gene Dosage Changes in the GCK Gene not Detected by Sanger DNA Sequencing in Two Patients with Phenotypic MODY 2
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HRP0092P1-320

Assessment of Vascular Endothelial Dysfunction Using Brachial Artery Flow Mediated Dilatation and Carotid Intima Media Thickness in Children and Adolescents with Type 1 Diabetes
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HRP0092P1-321

A Case of Late-Onset Monogenic Diabetes Due to a Homozygous Variant in the GCK Gene
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HRP0092P1-322

Neonatal Diabetes and Glis3 Mutation: A New Phenotype
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HRP0092P1-323

Diabetes Type 2 in Non-Obese Neurologically Impaired Children and Adolescents: A New Emerging Entity?
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HRP0092P1-324

Cataract in Type 1 Diabetes Mellitus Patients- a Nationwide Population-Based Study
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HRP0092P1-325

Association of CTLA-4 Gene with the Familial Diabetes Mellitus
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HRP0092P1-326

Copy Number Variation (CNV) Sequencing Identifies a Novel Mutation of the Glucokinase Gene in Maturity-Onset Diabetes of the Young
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HRP0092P1-327

The Paediatric Diabetes Service in England and Wales  Learning from Sweden's Improvement Journey.
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HRP0092P1-328

Creating a Neural Network Model Based on Glycemic Variability Indices to Predict the Degree of Compensation for Type 1 Diabetes
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HRP0092P1-329

Evaluation of AGP Reports in Patients with Type 1 Diabetes Using Intermittently Viewed Continuous Glucose Measurement System (iCGM)
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Abstract PDF
HRP0092P1-330

Evaluation of Clinical, Laboratory and Therapeutic Features and Long Term Follow-up Results in 44 Cases with Genetic Diagnosis of MODY; Single Center Experience
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HRP0092P1-331

Design and Implementation of an Integral System of Clinical Follow-Up and Glucose Monitoring in Children Affected of Type 1 Diabetes, in Andalusia
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HRP0092P1-332

Targeted Next-Generation Sequencing Demonstrates High Frequency of MODY in Russian Children.
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HRP0092P1-335

The Relationship Between Serum Neurotensin Levels and Metabolic Parameters and Eating Behavior in Obese Children
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HRP0092P1-337

How does Clusters of Parental Characteristics Influences Offspring Adiposity: A Prospective Study
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HRP0092P1-338

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

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HRP0092P1-339

Elevated High-Sensitivity C-Reactive Protein Level is Associated with Prediabetes and Adiposity in Korean Children and Adolescents.
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HRP0092P1-341

ANGPTL2 and ANGPTL3 in Children with Obesity and Metabolic Syndrome
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HRP0092P1-342

Can Increased First Hour Glucose Concentration in OGTT Be a New Indicator in Projecting Metabolic Profile?
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HRP0092P1-343

Perinatal Features of Prader-Willi Syndrome: A Chinese Cohort
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HRP0092P1-346

Non-Invasive Assessment of Liver Steatosis: Usefulness of Elastography in Obese Children  a Pilot Study.
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HRP0092P1-347

Precocious Pubarche in Spinal Muscular Atrophy Patients with Severe Sarcopenia
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HRP0092P1-348

Evaluation of the Relationship Between Serum Uric Acid Level and Cardiometabolic Risk in Obese Children and Adolescents
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HRP0092P1-349

Prevalence of Dyslipidemia in Korean Youth Over 10 Years: Data from the Korea National Health and Nutrition Examination Survey 2008-2017
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HRP0092P1-350

Metabolic Risk in Long-Term Survivors of Childhood Acute Lymphoblastic Leukemia
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HRP0092P1-351

Congenital Generalized Lipodystrophy Type 4 - New Mutation in the CAVIN1 Gene
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HRP0092P1-352

Paediatric Patients with Type 1 Diabetes Mellitus Exhibit Reduced Brown Adipose Tissue Heat Signature Following Cold Stimulation
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HRP0092P1-354

Association Between Adiposity Measures and Metabolic Variables in Children and Adolescentswith Obesity
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HRP0092P1-355

A Comparison of Insulin Resistance Indices: HOMA and Belfiore in 6-8-Year-Old, Properly Growing Children, Born Small for Gestational Age
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HRP0092P1-356

The «Double Diabetes» in Adolescent with Prader-Willi Syndrome.
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HRP0092P1-357

Evaluation of Body Composition and Resting Metabolic Rate in Adolescents with KS
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HRP0092P1-358

Relationship Between RBP4 Level and Two of its Gene Polymorphisms with Body Composition and Metabolic Profile in Obese Children
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HRP0092P1-359

Insulin-Like Growth Factor 2 in Pediatric Gliomas: Expression, Intracellular Localization and Association with Clinical Outcome
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HRP0092P1-360

Prevalence of Children Born Small for Gestational Age with Short Stature who Qualify for Growth Hormone Treatment: A Preliminary Population-Based Study
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HRP0092P1-361

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
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HRP0092P1-363

Metabolism of Somapacitan, a Long-Acting Growth Hormone Derivative, in Human Subjects
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HRP0092P1-364

GH Values in Serum and Blood Spots on Filter Paper Samples in Neonates Until 30 Days of Life by Electrochemiluminescence (ECLIA).
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HRP0092P1-365

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
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HRP0092P1-366

Glomerular Filtration Rate in Young Adults Born SGA: A 5-Year Longitudinal Study after Cessation of GH Treatment.
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HRP0092P1-367

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.
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HRP0092P1-369

Detection and Referral of Children with Short Stature in Serbia - the Impact of Electronic Growth Charts
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HRP0092P1-370

Challenges Experienced in Delivering Growth Hormone Therapy in Children's with Prader Willi Syndrome in Birmingham Children's Hospital.
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HRP0092P1-371

Growth Hormone Deficiency (GHD): Assessing Parent Burden for Child Growth Hormone Deficiency Treatment: The Growth Hormone Deficiency - Parent Treatment Burden Measure (GHD-PTB)
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HRP0092P1-373

Matrix Metalloproteinases, their Inhibitors and Neurotrophic Factors as Indicators of Cardiometabolic Risk in Turner Syndrome Girls
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HRP0092P1-374

Growth in the First Ten Years after Antiretroviral Therapy Initiation Among HIV-Infected Children in the CoRISpe Spanish Pediatric Cohort.
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HRP0092P1-375

SOAR Study: New Approaches to Managing Social Skills Deficits in Turner Syndrome
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HRP0092P1-376

Noonan Syndrome (NS) Spectrum Panels should Include Mutations in LZTR1 Gene
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HRP0092P1-377

International Consensus: Ovarian Tissue Cryopreservation in Young Turner Syndrome Patients. Outcomes of an Ethical Delphi Study Including 55 Experts from 16 Different Countries.
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HRP0092P1-378

Vascular Anomalies and Aortic Dilatation in Turner Syndrome Study in a Large Cohort of Young-Adult Patients
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HRP0092P1-379

Adult Height Prediction by Bone Age Determination in Children with Idiopathic Growth Hormone Deficiency (IGHD): Analysis of KIGS Data
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HRP0092P1-380

A New Model of Adult Height Prediction Validated in Boys with Constitutional Delay of Growth and Puberty
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HRP0092P1-381

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.
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HRP0092P1-382

Nutritional Requirements in Prader Willi Syndrome Children Treated with Growth Hormone Under Two Years of Age
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HRP0092P1-383

Cardiovascular Anomalies and Association with Karyotypes in Turner Syndrome in Taiwan: One Medical Center Experience
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HRP0092P1-384

Pubertal Induction Amongst Girls with Turner Syndrome: A Review of Changing Practice Over 10 Years.
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HRP0092P1-386

Prevalence of Copy Number Variations (CNVs) in a Cohort of SGA Children with Persistent short Stature Associated with Additional Clinical Features.
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HRP0092P1-388

Is there a QTc Interval Prolongation in Girls and Women with Turner Syndrome?
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HRP0092P1-389

Eight Years of Growth Hormone Treatment in a Patient with Schaaf-Yang Syndrome
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HRP0092P1-390

Genetic Evaluation of Idiopathic Short Stature
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HRP0092P1-391

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.
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HRP0092P1-392

Do Children and Adolescents with Idiopathic short Stature show Postural Alterations? Possible Influence of SHOX Haploinsufficiency in a Pilot Study
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HRP0092P1-393

Evaluation of Body Composition and Resting Metabolic Rate in Children with Growth Hormone Deficiency
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HRP0092P1-395

Presentation and Diagnosis of Childhood Onset Combined Pituitary Hormone Deficiency: A Single Center Experience from Over 30 Years.
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HRP0092P1-397

Questioning the Value of Brain MRIs in the Evaluation of Children with Isolated Growth Hormone Deficiency
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HRP0092P1-398

Postoperative Quality of Life in Children and Adolescents with Craniopharyngioma  Results of the Prospective Multicenter Trial KRANIOPHARYNGEOM 2007
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HRP0092P1-399

Pubertal Events, Reproductive and Growth Hormones and Predictive Factors in Healthy Girls with Transient Thelarche.
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HRP0092P1-400

Plasma Copeptin Distribution in the Pediatric Age: A Useful Diagnostic Tool for AVP-Related Disorders
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HRP0092P1-401

Management and Treatment Outcome of Childhood-Onset Craniopharyngioma (CP) in Italy: Multicentre Collection of 117 Cases
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HRP0092P1-402

Evaluation of Brain Mri Lesions in 381 Girls with Central Precocious Puberty
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HRP0092P1-403

Xanthomatous Hypophysitis: A Rare Case in a Paediatric Patient
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HRP0092P1-404

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
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HRP0092P1-406

Tolvaptan for Management of Intractable Salt and Water Imbalance in a Case with Suprasellar Tumor after Surgery
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HRP0092P1-407

No Association Between Serum Level of NPTX 1 and MKRN3 in Central Precocious Puberty
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HRP0092P1-408

Training in Pubertal Assessment  First Step to the Observational Pilot Study PROSPEL (Premier Observatoire des Stades Pubertaires en Libéral)
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HRP0092P1-409

Long-Term Outcome in Young Women Treated for Central Precocious Puberty
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HRP0092P1-410

Sertoli Cell Function after Chemotherapy in Boys with Hematologic Malignancies
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HRP0092P1-412

WES Analysis of a Cohort of 94 Patients Presenting with 46,XY and 46,XX DSD
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HRP0092P1-413

Assessment of the Function of Lower Urinary Tract Following Feminizing Genitoplasty in Females with Congenital Adrenal Hyperplasia
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HRP0092P1-414

Gonadal Insufficiency and Affecting Factors in Patients with Bone MarrowTransplantation(BMT) for Non-malignantIndications in Childhood or Adolescence
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HRP0092P1-415

Clinical and Molecular Characteristics of Russian Patients with 46,XY DSD due to NR5A1 Gene Mutations.
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HRP0092P1-416

Creating a Clinical Evaluation System for Simple and Comprehensive Scoring of Differences/Disorders of Sexual Development
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HRP0092P1-418

Epidemiology of Diagnoses of Sex Development Disorders Based on the Registry of Rare Diseases, in a Large Area of North-Eastern Italy
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HRP0092P1-419

Premature Ovarian Insufficiency in Women after Treatment for Childhoodcancer is a Risk Factor for Metabolic Syndrome
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HRP0092P1-420

The Genetic and Clinical Characteristic of Pediatric Patients with Congenital Hypothyroidism Gland In-Situ
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HRP0092P1-421

Zinc Transporter 8 (ZnT8) as a New Autoantigen in Thyroid Tissue  Preliminary Data
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HRP0092P1-422

Prospective Evaluation of Autoimmune and Non-Autoimmune Subclinical Hypothyroidism in a Large Cohort of Children and Adolescents with Down Syndrome
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HRP0092P1-423

Congenital Hypothyroidism (CH) Detected by the Second Newborn Screening in Lombardia Region: Incidence and Evolution of CH
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HRP0092P1-424

Transition for Patients with Chronic Thyroid Diseases
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HRP0092P1-425

Maternally Inherited Resistance to Thyroid Hormones with Discordant Postnatal Phenotypes in Two Infant Brothers
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HRP0092P1-426

A Rare Case of Familial Heterozygous Thyroid Hormone Receptor Beta (THRB) Mutation Presenting with Dilated Cardiomyopathy
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HRP0092P1-427

Acquired Hypothyroidism in a Toddler: An Unusual Presentation of Langerhans Cell Histiocytosis
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HRP0092P1-428

Anti-Gastric Parietal Cells Antibodies for Autoimmune Gastritis Screening: A Follow-Up Study in Young Patients with Autoimmune Thyroid Disease.
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HRP0092P1-429

Genetic Evaluation of Congenital Hypothyroidism with Gland-In-Situ Using Targeted Exome Sequencing
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HRP0092P1-430

Clinical Characteristics and Long-Term Follow-Up of Patients with Congenital Hypothyroidism (CH) due to Thyroid Peroxidase (TPO) Gene Mutations
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HRP0092P1-431

The Relationship Between Perfluoroalkyl Compounds Concentrations at Ages 2, 4, and 6 Years and Thyroid Function in Early Childhood: A Prospective Cohort Study
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HRP0092P1-432

Levothyroxine Effect on Thyroid Volume in Children with Autoimmune Hashimoto Thyroiditis (AHT) Presenting Subclinical (SH) or Overt (Oh) Hypothyroidism
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HRP0092LB-1

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
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HRP0092LB-3

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
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HRP0092LB-5

Height Curves and Height SDS in ADHD Children Measured Before and After Stimulant Treatment are not Affected - Observation Study in 7172 ADHD Children
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HRP0092LB-7

Long-Term Evaluation of Ovarian Function and Follicular Reserve in Patients with Malignant Diseases Treated with Chemotherapy in Prepubertal or Pubertal Age
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HRP0092LB-8

Detection of Cardiomyopathy in Egyptian Children and Adolescents with Longstanding Obesity Using Cardiac Marker NT-pro PNB and Speckled Tracking Echocardiography
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HRP0092LB-9

Left Ventricular Mass Index and Cardiovascular Function in Adolescents Born Small for Gestational Age (SGA)
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HRP0092LB-11

Height in Inborn Errors of Metabolism Requiring Hypoprotidic Diet: A Longitudinal Follow Up Study About 213 Patients
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HRP0092LB-12

Thyroid Function in Neonates Conceived After Hysterosalpingography with Iodinated Contrast Media
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HRP0092LB-13

Gut Hormones Secretion Across Clusters of Metabolic Syndrome in Obese Prepubertal Children
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HRP0092LB-14

Prenatal Smoke-Exposure is Associated with Increased Anogenital Distance in Female Infants
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HRP0092LB-15

Efficacy of 3-Monthly Compare to Monthly Depot GnRH Agonist (Triptorelin Pamoate) in the Treatment of Girls with Central Precocious Puberty in Korea
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HRP0092LB-17

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
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HRP0092LB-18

Exploratory Case-Control Study on ACE2 Expression in Children with Short Stature
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HRP0092LB-19

CDX2 Polymorphism of VDR Gene and Lipid Profile in Patients Treated for Acute Lymphoblastic Leukemia During Childhood
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HRP0092LB-20

IIntroduction of Flash Glucose Monitoring in Children with Type 1 Diabetes: Experience of a Single-Centre in Spain
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HRP0092LB-22

Two Novel Mutations of The LHX3 Gene Associated with a Severe Phenotype Involving Endocrine, Nervous and Skeletal Systems
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HRP0092LB-23

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
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HRP0092LB-24

Abdominal Adiposity and Total Body Fat as Predictors of Cardiometabolic Health in Pre-Pubertal and Pubertal Youth
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HRP0092LB-25

Low Trabecular Bone Score in Children with Inflammatory Bowel Diseases
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HRP0092LB-26

Dramatic Clinical Response to Lenvatinib in One Pediatric Patient with Advanced Metastatic Papillary Thyroid Carcinoma
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HRP0092LB-27

Does Karyotyping and in situ Hybridization from Three Different Germ Layers Elucidate Low Bone Mineral Density in Turner Syndrome?
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HRP0092LB-28

The Volumetric Changes in the Olfactory Bulb Depend on Body Mass Index
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HRP0092P2-1

Gender Identity, Sexual Orientation and Quality of Life in Women with Non-classic Congenital Adrenal Hyperplasia
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HRP0092P2-2

CYP11A1 (Side-chain Cleavage Enzyme) Defect in Three Brothers Causing Glucocorticoid and Mineralocorticoid Deficiency and Development of Testicular Adrenal Rest Testicular Tumour
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HRP0092P2-3

Contraceptives in Female Adolescents with 21-hydroxylase Deficiency (CAH) - a way to Optimize Treatment with Respect to Androgen Excess? A Pilot Study
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HRP0092P2-4

Bone Age Advancement in Prepubertal Children with Premature Adrenarche
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HRP0092P2-5

Clinical Phenotype and Genotype Association in Patients with 21-hydroxylase Deficiency
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HRP0092P2-6

Corticosteroid Use: Practices and Attitudes of Pediatricians
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HRP0092P2-7

Updates on Genotype and Phenotype of Vietnamese Patients with X-Linked Adrenoleukodystrophy
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HRP0092P2-8

Novel TBX19 Mutation as Cause of Hypoglicemia in Two Siblings
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HRP0092P2-9

The Clinical Polymorphism and Variability of X-linked Adrenoleukodystrophy in One Russian Family
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HRP0092P2-10

Functional Adrenocortical Oncocytoma  a Rare Cause of Progressive Virilization and Secondary Amenorrhea
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HRP0092P2-11

Long-term Prednisone versus Hydrocortisone Treatment in Children with Classic Congenital Adrenal Hyperplasia (CAH): A Controlled Study
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HRP0092P2-12

A Case of X-linked Adrenoleukodystrophy Presenting with Primary Adrenal Insufficiency and Normal VLCFA
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HRP0092P2-13

Different Potent Glucocorticoids, Different Routes of Exposure but The Same Result: Iatrogenic Cushing's syndrome and Adrenal Insufficiency
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HRP0092P2-14

Differences Between Normal-bmi Girls with Premature Adrenarche and Overweight or Obese Girls with Premature Adrenarche
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HRP0092P2-15

Rare Causes of Primary Adrenal Insufficiency at King Faisal Specialist Hospital Retrospective Study
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HRP0092P2-16

A Case of Infantile Cushing's Syndrome from McCune Albright Syndrome: The Importance of Multiple-Site Sampling for Genetic Testing
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HRP0092P2-17

Duodenal Web Presenting as Pseuhypoaldosteronism in Infancy
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HRP0092P2-18

A Rare Case of Pseudohypoaldosteronism in a Neonate Secondary to Congenital Hydrometrocolpos
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HRP0092P2-19

Hyperandrogenism in a 13-year-old Girl due to Glucocorticoid Receptor Mutation
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HRP0092P2-20

Polydipsia, Hyponatremia and a Biochemical Profile of Aldosterone Synthase Deficiency
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HRP0092P2-21

Fludrocortisone Treatment in a Child with Postural Orthostatic Tachycardia Syndrome (POTS): A Case Report
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HRP0092P2-23

"Girls with Idiopathic Premature Adrenarche Achieve Normal Adult Height"
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HRP0092P2-24

Adult Height and Growth Pattern in Patients with Classic Congenital Adrenal Hyperplasia
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HRP0092P2-25

Cushing Syndrome due to an Adrenacortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome
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HRP0092P2-26

Successful Parathyroidectomy with Intraoperative Parathyroid Hormone Monitoring in a Neonate with Severe Primary Hyperparathyroidism due to a Novel CASR Mutation
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HRP0092P2-27

The First Case Report of SEMD-JL1 in China
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HRP0092P2-29

Clinical and Genetic Characteristics of Pseudohypoparathyroidism Type 1A in Children Based on Single-center Cohort Study
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HRP0092P2-30

A Rare case of Neonatal Hypocalciuric Hypercalcemia Complicated with Arrhythmia
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HRP0092P2-31

Experience of Burosumab Therapy in Four Children with X-linked Hypophosphataemia in Saudi Arabia
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HRP0092P2-32

Pediatric Patients with Heterozygous ALPL Mutation show a Broad Clinical Phenotype
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HRP0092P2-33

Growth and Bone Mineral Density in Egyptian Children with Congenital Adrenal Hyperplasia on Glucocorticoid Replacement Therapy; A Single Center Study
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HRP0092P2-34

Chronic Bone Disease in Pediatric Sickle Cell Disease Including a Case of Successful Bisphosphonate Therapy
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HRP0092P2-35

Clinical and Genetic Characteristics of 168 Russian Patients with Hypophosphatemic Rickets
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HRP0092P2-36

A 10-year-old Girl with Primary Hypoparathyroidism and Systemic Lupus Erythematosus (SLE)
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HRP0092P2-37

An Unusual Case of Hyperparathyroidism: Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (FHHNC) Associated with Mutations in CLDN19
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HRP0092P2-38

Skeletal Maturity and Growth in children with Type 1 Diabetes
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HRP0092P2-39

Bone Mineral Status in Adults with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
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HRP0092P2-40

Reduced Bone Mineral Density in Children with Inflammatory Bowel Disease without Exposure to Corticosteroid Treatment
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HRP0092P2-41

A Clinical Dilemma in the Detection of Paediatric Hypophosphataemia
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HRP0092P2-43

A Rare Form of Vitamin D Receptors Dysfunction (vitamin D-dependent Rickets Type II) with Alopecia. A Case Report
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HRP0092P2-44

Cinacalcet Experience in Hypercalcemia Due to CaSR Mutation
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HRP0092P2-45

Two Siblings with Hypophosphatemic Rickets: SLC34A3 Gene Mutations with Different Clinical Phenotypes
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HRP0092P2-46

Seasonal 25-hydroxy Vitamin D3 Variations in School-aged Children from Santiago de Chile
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HRP0092P2-49

Successful Treatment with Enzyme Replacement Therapy in a Girl with Severe Infantile Hypophosphatasia
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HRP0092P2-50

Bone Mineral Density in Children with Type 1 Diabetes Mellitus (T1DM) and Analysis of Possible Factors Affecting Their Bone Health; A controlled study
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HRP0092P2-51

Perinatal form Hypophosphatasia Caused by a Novel Large Duplication of ALPL Gene and two year follow-up under Enzyme Replacement Therapy; A case report
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HRP0092P2-52

A rare cause of hypophosphatemia: Raine Syndrome
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HRP0092P2-53

Idiopathic Infantile Hypercalcemia: Mutations in SLC34A1 and CYP24A1 in Two Siblings and Fathers
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HRP0092P2-55

A Novel Missense COL10A1 Mutation Identified by Next Generation Sequencing in a Chinese Pedigree with Schmid Metaphyseal Chondrodysplasia
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HRP0092P2-56

a case report of a girl with short stature has laron syndrome and spondyloepimetaphyseal dysplasia
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HRP0092P2-57

A Novel Mutation of Phex Gene Inducing X-Linked Hypophosphatemia Rickets, A Case Report
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HRP0092P2-58

Skeleton Muscles and Tissues Metabolic Activity in Greek Adolescent PCOS
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HRP0092P2-59

Spondyloocular Syndrome: Presentation of Two Siblings Diagnosed with The Rare Disease and The Results of Pamidronate Therapy
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HRP0092P2-60

Clinical and Genetic Characterization of Tunisian Children with Hereditary Hypophosphatemic rickets (HHR).
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HRP0092P2-61

Osteogenesis Imperfecta: Genetic Evaluation
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HRP0092P2-62

The Effect of Carbohydrate Recognition and Counting Ability on Glycemic Control in Pediatric Patients with Type 1 Diabetes
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HRP0092P2-63

A Rare Case of Syndromic Diabetes due to an INSR Pathogenic Variant
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HRP0092P2-64

Autoimmune Thyroid Diseases in Children and Adolescents with Maturity Onset Diabetes of the Young
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HRP0092P2-66

New Mutation of the PDX-1 Gene Causes MODY Type 4 Diabetes in a 17 year old girl with Good Response to Oral Antidiabetics
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HRP0092P2-68

Pancreatic β Cell Function and its Relationship with Iron Overload in Patients with β-Thalassemia Major
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HRP0092P2-69

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
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HRP0092P2-70

Evaluation of β-cell Function in Young MODY Patients using a Mixed Meal Tolerance Test
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HRP0092P2-71

The Effect of Different Forms of Maternal Dysglycemia on the occurrence of Neonatal Hypoglycemia in babies admitted to NICU.
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HRP0092P2-72

Adropin, Afamin And Neudesin - Novel Biomarkers of Type 1 Diabetes Mellitus in Children
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HRP0092P2-73

Prevalence, Time Trend and Predictors of Celiac Disease in Type 1 Diabetes
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HRP0092P2-74

Impact of the Flash Glucose Monitoring System on Children with Type 1 Diabetes After the First Year of Using in Systematic Way
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HRP0092P2-75

Insulin Treatment of Cystic Fibrosis Related Diabetes (CFRD) on BMI and Respiratory Function
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HRP0092P2-76

Coexistence of Medium chain acyl-CoA dehydrogenase deficiency (MCADD) and Type 1 diabetes (T1D): A management challenge
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HRP0092P2-77

Education in type 1 Diabetes Mellitus (T1D): what do Educators Really Know? A Tunisian Multicenter Study among Young Doctors, Nurses and Nutritionnists
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HRP0092P2-78

A Case of an Infant with Congenital Hyperinsulinism Complicated by Diabetic Ketoacidosis during Treatment
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HRP0092P2-80

Effect of Multiple dose Insulin on Glycaemic Control and Adiposity in Children and Adolescents with Type 1 Diabetes; a Sri Lankan Experience
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HRP0092P2-82

Thiamine Responsive Megaloblastic Anemia Syndrome with Restrictive Cardiomyopathy: A case report
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HRP0092P2-83

17q12 Deletion and a Family History of Diabetes
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HRP0092P2-84

An Unusual Presentation of Type 1 Diabetes
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HRP0092P2-85

Clinical Characteristics and Treatment Outcomes in Patients with Autoantibody-negative Ketosis-prone Diabetes
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HRP0092P2-86

Factors Influencing the Formation and Support of the Motivation to Self-control of Adolescents with Type I Diabetes Mellitus
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HRP0092P2-87

Glycemic Control in Egyptian Adolescent Girls with Type 1 DM
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HRP0092P2-88

A Qualitative Study Investigating the Experiences of Using Solution Focused Therapy in a Paediatrics Diabetes Team
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HRP0092P2-90

Neonatal Diabetes in Two Siblings with Foxp3 Variant
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HRP0092P2-91

A Novel Variant of the WFS1 Gene with Dominant Inheritance Causing Wolfram-like Syndrome
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HRP0092P2-92

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

Abstract PDF
HRP0092P2-93

The Growth Hormone Treatment and Carbohydrate Metabolism in Children Born Small for Gestational Age
Direct

Abstract PDF
HRP0092P2-94

Empirical Sulphonyurea in Neonatal Diabetes: Results from a aTertiary Care Centre
Direct

Abstract PDF
HRP0092P2-95

Diabetes Mellitus, Severe Acanthosis Nigricans and Short Stature: a Rare Association in Chinese Children
Direct

Abstract PDF
HRP0092P2-96

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

Abstract PDF
HRP0092P2-97

Does Commencing on an Insulin Pump Improve Glycaemic Control in Paediatric Patients?
Direct

Abstract PDF
HRP0092P2-98

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

Abstract PDF
HRP0092P2-99

A Case of Neonatal Diabetes Due to Newly Defined Mutation in the GLIS 3 Gene
Direct

Abstract PDF
HRP0092P2-100

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

Abstract PDF
HRP0092P2-101

Evaluation of the Effect of Knowledge Levels of Adolescents Diagnosed with Type 1 Diabetes Melllitus on Hba1c and Life Quality Score
Direct

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HRP0092P2-102

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

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HRP0092P2-103

Evaluation of the Association of Glutamic Acid Decarboxylase Antibody and Limbic Encephalitis in Children with Type 1 Diabetes Mellitus
Direct

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HRP0092P2-104

Insulin Pump Therapy Implementation in Uzbekistan
Direct

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HRP0092P2-105

Cardiopulmonary exercise testing, body composition and metabolic status in young adults after allogeneic human stem cell transplantation for hematological malignancy in childhood
Direct

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HRP0092P2-106

School-age Children Awareness of Seriousness of Obesity Problem, Health-related Outcomes and Effectiveness of Self-control Preventive Strategies
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HRP0092P2-107

Childhood Obesity and Iron Metabolism
Direct

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HRP0092P2-108

Effectiveness of Multidisciplinary Outpatient Approach in the Management of Paediatric Obesity
Direct

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HRP0092P2-109

Metabolic Syndrome in Children and Adolescents who Survived After Childhood Cancer
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HRP0092P2-110

Pubertal Milestones and Related Hormonal Changes Among Children with Obesity
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HRP0092P2-112

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
Direct

Abstract PDF
HRP0092P2-113

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

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HRP0092P2-115

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
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HRP0092P2-116

Nonalcoholic Fatty Liver Disease in Pediatric Obese Patients
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HRP0092P2-117

Trends in Childhood Obesity, Underweight and Short Stature Among Urban School Children in Romania
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HRP0092P2-118

Impact of a Comprehensive Program, on Prevalence of Childhood Obesity in Andalusia, Spain
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HRP0092P2-119

Evaluation of Fetuin-A Level and Related Factors in Obese Adolescents
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HRP0092P2-120

Prevalence of Obesity among Infants Presenting with Intussusception
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HRP0092P2-121

A Non-invasive Model for Detection of the Metabolic Syndrome in Children and Adolescents
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HRP0092P2-122

Insulin-like Growth Factor-1 and Binding Protein-3 in Children with Metabolic Syndrome
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HRP0092P2-123

Overweight, Obesity and Hypertension among Adolescents  the Impact of Immigration and a Acculturation
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HRP0092P2-125

Clinical Features and Genetic Analysis of Childhood Dyslipidemia
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HRP0092P2-126

Tracking Body Mass Index From Infancy into Childhood
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HRP0092P2-127

The bilirubin/triglycerides Ratio Predicts Changes over time in Glycated Hemoglobin in Prepubertal Healthy Children
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HRP0092P2-128

Is one year of Diet and Physical Activity Program for Obese Children Enough to Revert the Metabolic Disorders?
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HRP0092P2-129

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
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HRP0092P2-130

Severe Obesity  Much More Than an Unhealthy Lifestyle
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HRP0092P2-131

Serum 25-hydroxyvitamin D Levels and Insulin Sensitivity Across Pubertal Stages in Obese Children
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HRP0092P2-132

Association Between TSH and Metabolic Syndrome in Obese Children and Adolescents
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HRP0092P2-133

Primary Hyperlipidemia in Children: Experience of 11 years from a Referral Center in Vietnam
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HRP0092P2-134

Tumor Necrosis Factor Alpha in Metabolic Syndrome Development in Children
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HRP0092P2-135

Clinical and Cytogenetic Analysis on Two Chinese Familial Cases of Prader-Willi Syndrome with Multiple Affected Patients
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HRP0092P2-136

Insulin Resistance and Impaired Glucose Tolerance in Overweight/Obese Adolescents Attending an Obesity Clinic in Belgium
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HRP0092P2-137

Clinical Characteristics and Response to Growth Hormone Treatment in Patients with Prader-Willi Syndrome
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HRP0092P2-139

The Prevalence of Elevated Blood Pressure and Hypertension in Korean Adolescents, based on the Guidelines of Endocrine Society and American Academy of Pediatrics
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HRP0092P2-140

Pedobesity: Development of Intelligent Multi-level Information Systems and Specialized Artificial Intelligence Algorithms for Personalized Management of Obesity in Childhood and Adolescence
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HRP0092P2-141

Metabolic Syndrome Risk Assessment in Indian children and Adolescents
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HRP0092P2-142

Vitamin D Status in Obese Children and its Relationship with Leptin and Adiponectin
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HRP0092P2-143

Two Siblings with Tyrosinaemia Type 1 and Transient Hyperinsulinaemic Hypoglycaemia
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HRP0092P2-144

Glucagon Therapy in Preterm Infants with Hyperinsulinemic Hypoglycaemia
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HRP0092P2-145

Neonatal Hypo-ketotic Hypoglycemia Secondary to Transient Hyperinsulinism. Diazoxide Responsiveness and Experience with Fasting Test after Treatment Withdrawal
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HRP0092P2-146

Severe Neonatal Hyperparathyroidism Due to a Novel Homozygous Mutation of the Calcium-Sensing Receptor (CaSR)
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HRP0092P2-147

A Rare Cause of Pediatric Hypoglycemia in a Boy: A Malignat Insulinoma
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HRP0092P2-149

Clinical and Genetic Characteristics of Patients with Hyperinsulinaemic Hypoglycaemia Diagnosed and Treated at a Tertiary Endocrine Center, a part of the ENDO-ERN
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HRP0092P2-150

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
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HRP0092P2-151

Refractory Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Imprinting Centre 1 Gain of Methylation: Severity Discordant to Genotype
Direct

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HRP0092P2-152

Congenital Hyperinsulinism due to Compound Heterozygous Mutations in ABCC8 Fully Responsive to Diazoxide Therapy
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HRP0092P2-153

Criteria for First-Year Growth Response to Growth Hormone Treatment in Prepubertal Children with Growth Hormone Deficiency: Do they Predict Final Height Outcome?
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HRP0092P2-154

Determinants of the Peak GH Response of the Glucagon Stimulation Test in Slowly Growing Children
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HRP0092P2-156

Growth Hormone Monotherapy Versus Combined GH and LHRH Analog in 2 Sisters with Short Stature, Early Pubertal Development, and Advanced Bone Age (BA)
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HRP0092P2-157

Long-Term Follow-Up of Three Patients with Isolated Growth Hormone Deficiency Type IA Withsustained Growth Response to rhGH
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HRP0092P2-158

Clinical and Genetic Characteristics of Eleven Korean Patients with Hypochondroplasia and Outcomes of Growth Hormone Therapy
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HRP0092P2-159

Growth Hormone Treatment Adherence in Latin American Patients: 2-Year Real World Data from the Easypod Connect eHealth Platform
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HRP0092P2-160

Metabolic Outcome in Adolescents with Growth Hormone Deficiency During Transition Phase
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HRP0092P2-161

The Influence of Pituitary MRI Findings on Clinical Presentation and Growth in GH-Treated Children with Congenital Hypopituitarism
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HRP0092P2-162

Metabolic Effects of Growth Hormone Treatment in Short Prepubertal Children: A Double-Blinded Randomized Clinical Trial
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HRP0092P2-163

Growth Response in Short Preterm- Born Children Small for Gestational Age in First Year of Growth Hormone Treatment
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HRP0092P2-164

Brain Magnetic Resonance Imaging in Children with Isolated Growth Hormone Deficiency and Idiopathic Short Stature Diagnoses
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HRP0092P2-165

The Clinical Significance of Post-Sleep Growth Hormone Levels in the Diagnosis of Growth Hormone Deficiency
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HRP0092P2-166

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
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HRP0092P2-167

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)
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HRP0092P2-170

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
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HRP0092P2-171

Final Height in GH-deficient Paediatric Patients: A Nationwide Experience
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HRP0092P2-172

Differences of Efficiency of Treatment of Isolated Growth Hormone Deficiency and Panhypopituitarism in Children in Real Clinical Practice
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HRP0092P2-173

Implementation of a Growth Disorders Related Twinning Program in Pediatric Endocrinology  is it Necessary and Feasible?
Direct

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HRP0092P2-174

Empirical Change of Practice in Treatment of Growth Hormone Deficient Patients in Order to Improve 1st Year Height Outcome
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HRP0092P2-175

The Impact of Growth Hormone Treatment in Patients with Noonan Syndrome and Growth Hormone Deficiency
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HRP0092P2-176

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
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HRP0092P2-177

Five Novel Variants of KMT2D/KDM6A Found in Seven Chinese Patients with Kabuki syndrome and a Literature Review of 39 Patients Reported in China
Direct

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HRP0092P2-178

Adult Height of Patients Enrolled in PATRO Children, An Ongoing Observational Study of the Long-term Safety And Effectiveness Of Omnitrope®
Direct

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HRP0092P2-179

Unusual Case of Patient with Klinefelter Syndrome with Shox Deletion Born to the Mother with Leri-weill Dyschondrosteosis
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HRP0092P2-180

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
Direct

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HRP0092P2-182

Auditory Phenotypes and Dynamics of Hearing Thresholds in 246 Turner Syndrome Females
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HRP0092P2-183

The Prevalence of Celiac Disease (CD) in Children with Type 1 Diabetes Mellitus (T1D); Does CD Adversely Affect Linear Growth in these Children?
Direct

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HRP0092P2-184

Effect of Gonadotropin-Releasing Hormone Agonists on Auxological Outcomes of Korean Boys with Central Precocious Puberty and Early Puberty
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HRP0092P2-186

Clinical Features in a Patient with Turner Syndrome and Pericentric Inversion of Chromosome 9
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HRP0092P2-187

"Transition Readiness in Girls and Young Women with Turner Syndrome  are they Less Ready?" Associations between Transition Readiness and Diagnosis
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HRP0092P2-188

Clinical and Molecular Genetic Characterizations of Five Patients Harboring Mutations in the GNAS Gene: A Case Series and Literature Review
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HRP0092P2-189

Anophthalmia, Micrognathia, Combined Pituitary Hormone Deficiency, Severe Growth Retardation and Liver Dysfunction Induced Levothyroxine Sodium Powder in a Boy with Microdeletion of 14q22q23
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HRP0092P2-190

Growth Hormone Therapy in Patients with Noonan Syndrome
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HRP0092P2-192

Shox-Haploinsufficiency Intra-Familial Phenotipic Variability and the Impact on Final Height: Report of a Pedigree
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HRP0092P2-193

Linear Growth of Children with Celiac Disease (CD) after the First Two Years on a Gluten-Free Diet (GFD); A Controlled Study
Direct

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HRP0092P2-194

Growth Hormone Treatment Adherence in Patients from an Emerging Economy Country: 1-Year Real-World Data from the Easypod Connect Ehealth Platform
Direct

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HRP0092P2-195

The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation
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HRP0092P2-196

Klinefelter Syndrome Associated with Short Stature Due to Iatrogenic Cushing
Direct

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HRP0092P2-198

Evaluation of Diagnosis, Follow-up and Treatment Results of Growth Hormone in Rare Diseases; 10 Year Single Center Experience
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HRP0092P2-200

Endocrine Features of Schaaf-Yang Syndrome. Case Report
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HRP0092P2-201

Papillary Thyroid Cancer in a 17-Years Old Girl with a Late-Diagnosed Turner Syndrome
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HRP0092P2-202

The Applicability of the NH-Clinical Scoring System on Diagnosis of Iranian Children with SRS
Direct

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HRP0092P2-203

Clinical Manifestations & Molecular analysis of Thirteen Palestinian Families with Sanjad Sakatti Syndrome Revealing a Common Deletion Founder Effect and Another Two Novel Mutations
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HRP0092P2-204

Electromagnetic Fields Exposure in Adolescents: A Survey in 11-14 y Old Greek Students
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HRP0092P2-205

Subcutaneous Ossifications in Children - Think About AHO!
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HRP0092P2-206

Growth Outcomes in Growth Hormone Treated Indian Children with Celiac Disease
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HRP0092P2-208

Autoimmune Polyendocrine Sydrome Type I: A Neuroendocrine Multi-Systemic Disease with a Variable Expressivity
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HRP0092P2-209

Endocrine Complications of Patients with Hepatic Type of Glycogen Storage Disease
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HRP0092P2-210

Autoimmune Thyroiditis and Autoimmune Hepatitis Presenting at Onset of Type 1 Diabetes (T1D)
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HRP0092P2-211

Ulnar Mammary Syndrome - A Case Report
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HRP0092P2-212

Unusual Ovary Formation in a Girl with McCune-Albright Syndrome
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HRP0092P2-213

Heart Rate Variability in Adolescent Polycystic Ovary Syndrome Greek Patients
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HRP0092P2-214

Celiac Disease and Endocrine Autoimmunity in Children and Adolescents
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HRP0092P2-215

Intestinal Ganglioneuromatosis as First Manifestation of Multiple Endocrine Neoplasia 2B in a Premature Girl
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HRP0092P2-217

Effect of Testosterone Enanthate Therapy on Adult Height, Genital Maturation, and Bone Mineral Density in Children and Adolescents with Male Hypogonadotropic Hypogonadism
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HRP0092P2-218

The Difference of Body Mass Index (BMI) Score Before and After Gonadotropin-Releasing Hormone Agonist (GnRHa) Treatment in Central Precocious Puberty Girls
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HRP0092P2-219

Aromatase Inhibitor Treatment in Patient with Beta-Human Chorionic Gonadotrophin Secreting Tumor and Gonadotropin-Independent Precocious Puberty
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HRP0092P2-220

Normalized Pubertal Tempo of Maturation and Pubertal Height Gain in Girls with MPHD, Using a Physiological Treatment Approach with Natural Estrogens & rhGH
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HRP0092P2-221

The Case of Congenital Hypopituitarism Due to Mutation POU1F1 in 3 Azerbaijani Newborn Boys
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HRP0092P2-222

Case Report of Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) Caused by Rare AVPR2 Gene Active Mutation
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HRP0092P2-223

Long Term Effects of GnRH Agonist Therapy on BMI in Girls with Idiopathic Central Precocious Puberty
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HRP0092P2-224

To Whom Should Central Nervous System Imaging be Performed in Girls with Central Precocious Puberty (CPP)?
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HRP0092P2-225

Unusual Presentation of McCune-Albright Syndrome in a 10-Year-Old Girl
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HRP0092P2-226

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
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HRP0092P2-227

Screening of Central Precocious Puberty (CPP) in Females: Efficacy of Morning Unstimulated Luteinizing Hormone (mLH) Levels
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HRP0092P2-228

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
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HRP0092P2-229

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
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HRP0092P2-230

The Incidence and Diagnostic Factors of Polydipsia and Polyuria: A Single Center Survey in Japan
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HRP0092P2-231

Macroprolactinoma Presenting with Pituitary Apoplexy Associated with Middle Cerebral Artery Infarction in an Adolescent Male
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HRP0092P2-232

Childhood Craniopharyngioma: Clinical Picture at Diagnosis in an Italian Multicentre Study
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HRP0092P2-234

Evaluation of Clinical Features and Treatment Responses of Cases with Hyperprolactinemia
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HRP0092P2-235

A Case of Gonadotropin-Independent Precocious Puberty Due to Germ Cell Tumor in the Frontal Lobe
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HRP0092P2-237

Heterozygous OTX2 Deletion in a Boy with Normal Eye Development and Normal Pituitary Function
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HRP0092P2-238

Risk Factors for Hypogonadism in Patients with β-Thalassemia Major: A Cross-Sectional Study
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HRP0092P2-239

Radiation Therapy for Children with Medulloblastoma: Growth and Thyroid Sequalae
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HRP0092P2-240

Bone Age Determination in Girls with Early Puberty and Limitations of Adult Height Prediction: Can Automated Evaluation (BoneXpert)be a Solution?
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HRP0092P2-241

Effect of Gonadotropin-Releasing Hormone Agonist Treatment on Final Adult Height in Boys with Idiopathic Central Precocious Puberty
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HRP0092P2-242

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
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HRP0092P2-243

A Case of Severe Recurrent Hypoglycemia After Traumatic Brain Injury
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HRP0092P2-244

The Evolving Role of Whole Exome Sequencing in the Diagnosis of Disorders of Sex Development (DSD)
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HRP0092P2-245

Etiological Structure Disorders of Sex Development 46,XY By One Center
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HRP0092P2-246

Comparison of Growth Status, Level of Blood Glucose and Lipid Metabolism in SGA and AGA Girls with Central Precocious Puberty
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HRP0092P2-247

Does the Anogenital Distance Predict Outcome of Hypospadias Repair?
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HRP0092P2-249

11-Oxygenated Androgens May be Related to the Virilization of Female External Genitalia Due to the Maternal Androgen-Producing Adrenal Tumor
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HRP0092P2-250

High Prevalence GnRH Receptor Mutations in Russian Patients with Idiopathic Hypogonadotropic Hypogonadism
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HRP0092P2-251

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
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HRP0092P2-252

Clinical Evaluation of Newly Developed Scoring System for DSD (DSD-SS): Association of DSD-SS With Assigned Gender in 45,X/46,XY Mosaicism
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HRP0092P2-253

Complexities of Diagnosis in 17-Beta-Hydroxysteroid Dehydrogenase Deficiency and Implementation of Next Generation Sequencing in Guiding Management Decisions  Case Series of Six Patients
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HRP0092P2-254

Paediatric Health Assistance to Transsexual Minor in the Multidisciplinary Care Unit of the Basque Country (Spain)
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HRP0092P2-256

A Clinical and Cytogenetic Study of Patients with Disorders of Sex Development (DSDs) Associated with Congenital Anomalies or Recognizable Syndromes
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HRP0092P2-257

Physical Changes, Laboratory Parameters and Bone Mineral Density During Testosterone Treatment in Adolescents with Gender Dysphoria
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HRP0092P2-258

Study of Autistic Features Among Children and Adolescents with Congenital Adrenal Hyperplasia
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HRP0092P2-259

Differences of Sex Development with Chromosomal Mosaicism: Histological Characterization and Immunohistochemistry Markers in Gonads During Childhood
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HRP0092P2-260

Heterozygous CYP11A1 Mutation Associated with 46XY Disorder of Sexual Differentiation and Mild Adrenal Insufficiency
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HRP0092P2-262

Etiologic Classification of 46, XX Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results
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HRP0092P2-263

Novel Genotype in Two Siblings with 5-Alpha-Reductase 2 Deficiency:Different Clinical Course Due to the Time of Diagnosis
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HRP0092P2-264

Ethical and Familial Dilemmas of Genitoplasty Encountered in Congenital Adrenal Hyperplasia
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HRP0092P2-265

Hormonal Assessment of Malformation Syndromes Associated with Disorders of Sex Development: Case Series of 9 Patients
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HRP0092P2-266

Family Perrault Syndrome in Two Tunisian Sisters
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HRP0092P2-267

An Intriguing Co-Occurrence of MURCS and VACTERL Association: A Case Report and Review of the Literature
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HRP0092P2-269

Pseudo-Precocious Puberty in Children Triggered by Incidental Transdermal Contamination with Topical Sex Steroids Through Parents
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HRP0092P2-270

Follow-up of Individuals with Gender Identity Disorders: A Long and Challenging Process
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HRP0092P2-271

Follow-Up of Two Similar Patients with Steroidogenic Factor-1 (SF-1/ NR5A1) Variants, in Two Different Eras
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HRP0092P2-272

Genetic Testing of DSD Patients in Ukraine
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HRP0092P2-273

Spectrum of Genital Abnormalities in Robinow Syndrome: Case Series
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HRP0092P2-274

MAMLD 1 Gene Mutation and 46 XY Sex Development Disorder: A Case Report
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HRP0092P2-275

46,XY Complete Gonadal Dysgenesis in a Familial Case with a Rare Mutation in the Desert Hedgehog (DHH) Gene
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HRP0092P2-276

Novel Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone
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HRP0092P2-277

Congenital Hypothyroidism: Neonatal SCREENING PROGRAM with T4 and TSH
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HRP0092P2-278

A 10- Year-Old Girl with Thyroid Hormone Resistance (βTHR)- Case Report
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HRP0092P2-279

Diagnosis of Central Congenital Hypothyroidism and Multiple Pituitary Deficiencies Through a Neonatal Screening Program
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HRP0092P2-280

Childhood Thyroid Cancer After Radi Oiodine Therapy
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HRP0092P2-281

Differential Diagnosis of Euthyroid Hyperthyroxinemia
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HRP0092P2-282

Treatment for Graves' Disease in Children and Adolescents: A Long-Term Retrospective Study at a Single Institution
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HRP0092P2-283

Changes of Thyroid Function in Girls with Central Precocious Puberty After 6-Month GnRH Agonist Treatment
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HRP0092P2-284

Papillary Thyroid Cancer Associated with Hyperthyroidism
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HRP0092P2-285

Serum PTH Does not Correlate with Their Serum Calcium Levels in Children and Adolescents with Hashimoto Thyroiditis
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HRP0092P2-286

Management of Childhood Thyroid Nodules in Children a Large Group of Cases From a Single Center
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HRP0092P2-287

Bone Homeostasis in Children with Subclinical Hypothyroidism: Effects of Two-years Treatment with Levothyoxine
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HRP0092P2-290

A Rare Combination- Brain Lung Thyroid Syndrome
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HRP0092P2-292

Thyroid Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus
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HRP0092P2-293

Analysis of Diabetes-Associated Autoantibodies in Children and Adolescents with Autoimmune Thyroid Diseases
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HRP0092P2-296

Progressive Thyroid Dysfunction in Infants with Down Syndrome; Trisomy 21 (DS): Effect on Linear Growth
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HRP0092P2-297

Evaluation of Elevated Serum Thyroid-Stimulating Hormone (TSH) in Children and Adolescents: A Single-Center Study in Uruguay
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HRP0092P2-298

Neonatal Hyperthyroidism: Our Centre's Experience
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HRP0092P2-299

Epidemiological Aspects of Pediatric Thyroid Disorders in Western Ukraine
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HRP0092P2-300

The Encephalopathy as Complication of Hashimoto Thyroiditis in Children: A Wide Variety of Clinical Manifestations
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HRP0092P2-301

Acute-Onset Peripheral Polyneuropathy in a 12-Year-Old Girl Due to Hashimoto Thyroiditis: Traps in the Diagnosis
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HRP0092P3-1

A Case of Cushing Syndrome in a Wilms' Tumour
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HRP0092P3-2

A Rare Cause of Primer Adrenal Insufficiency: NROB1 (DAX1) Mutation
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HRP0092P3-3

A 46, XX Patient with 21-OHD Diagnosed During the Etiologic Workup of Male Infertility
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HRP0092P3-4

A Female Infant with Severe Salt-Wasting due to Aldosterone Synthase Deficiency, Initially Mimicking Adrenal Insufficiency
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HRP0092P3-5

Can Early Prenatal Prednisone Treatment Reduce Virilization of CAH Female Newborn?
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HRP0092P3-7

Rare Case of Cortisol Producing Tumour in 14 Years Old Girl
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HRP0092P3-8

Typical Phenotype of Isolated Aldosterone Synthetase (AS) Deficiency in two Infants with Heterozygous AS Gene Mutation: Dilemma for Diagnosis
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HRP0092P3-9

Late Onset 11 Beta Hydroxylase Deficiency: Two Cases
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HRP0092P3-10

An Unusual Testicular Adrenal Rest Tumor localization in a 15-Year-Old Boy with Congenital Adrenal Hyperplasia
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HRP0092P3-11

Primary Adrenal Insufficiency in Sudanese Children (Clinical Presentation, Etiology and Diagnostic Challenges)
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HRP0092P3-12

Clinical Follow-Up of a Novel NR0B1 Mutation in a Case of Adrenal Hypoplasia Congenital
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HRP0092P3-13

Genotype and Phenotype, Growth Outcome in 33 Korean Patients with 21-Hydroxylase Deficiency
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HRP0092P3-14

One Case Report of Uighur Girl with Cushing Syndrome
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HRP0092P3-15

Nephrotic Syndrome Developed in a Girl With Lipoid Adrenal Hyperplasia due to StAR Gene Mutation  First Report
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HRP0092P3-16

Pneumocystis Jiroveci Pneumonitis Complicating Neonatal Cushing's Syndrome - the Therapeutic Dilemma
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HRP0092P3-17

Newborn Screening for Congenital Adrenal Hyperplasia: Should we Worry more about False Positives or False Negatives?
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HRP0092P3-18

The Unusual Adverse Side Effects of Super-Potent Topical Steroids
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HRP0092P3-19

A Case with Central Adrenal Insufficiency and Early Onset Obesity: Proopiomelanocortin Deficiency
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HRP0092P3-20

Short Synacthen Test in Children at Sultan Qaboos University Hospital; Reviewing the Sampling Times
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HRP0092P3-21

Pheochromocytoma in Children: A Case Report
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HRP0092P3-22

A Case with Congenital Adrenal Hyperplasia Diagnosed by Malnutrition
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HRP0092P3-23

Recurrent Hypoglycemia-Not Every Low Sugar is Hyperinsulinemia
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HRP0092P3-25

Unusual Association: Allgrove Syndrome and Hypopituitarism
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HRP0092P3-26

Title: Long-Term Outcome of Congenital Adrenal Hyperplasia Patients at KFSHRC-Saudi Arabia. Tertiary Center Experience
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HRP0092P3-27

A Boy with Adrenal Hypoplasia Congenita without External Genital Abnormalities
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HRP0092P3-28

Linear Growth in Children with COW Milk Allergy and their Response to Hypoallergenic Diet; Significant Catch-Up in the First 6 Months
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HRP0092P3-30

ENPP1 Hypophosphatemic Rickets in a 3.6 Years Old Italian Child
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HRP0092P3-31

A Case Study of X-linked Hypophosphataemia: The Effect of Conventional Therapy from Childhood to Adulthood in Saudi Arabia
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HRP0092P3-33

In Case of Osteogenesis Imperfecta Transmission in Pregnancy: Check Vitamine D and Calcium Status of the Mother
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HRP0092P3-35

Pseudohypoparathyroidism: Four Cases Reports
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HRP0092P3-36

A Case of Robinow Syndrome
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HRP0092P3-38

Mild Hypophosphatasia in a Family with a Novel Mutation in the ALPL Gene
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HRP0092P3-39

Uncommon Association of Hypoparathyroidism and Rendu-Osler Syndrome
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HRP0092P3-40

Barakat Syndrome (HDR Syndrome): Case Report
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HRP0092P3-41

Myelofibrosis in Severe Vitamin D Deficiency Rickets: A Case Report
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HRP0092P3-42

Congenital Hyperinsulinism in Kosova
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HRP0092P3-43

About a Case of Neonatal Hypocalcemia
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HRP0092P3-45

Acute Lymphoblastic Leukemia;Atypically Presenting with Sever Hypercalcemia in a Palestinian Child
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HRP0092P3-46

Growth Hormone Treatment of a Patient with X-Linked Hypophosphatemic Rickets Caused by PHEX Mutation: Effects on Linear Growth
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HRP0092P3-48

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
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HRP0092P3-49

Significance of the Early Marker of Nephrine Diabetic Nephropathy of the Uzbek Nationality with the First Type of Diabetes Mellitus
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HRP0092P3-50

Hybrid Diabetes with Good Response to Metformin in an Adolescent with Polyglandular Polyendocrinopathy (APS2)
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HRP0092P3-52

Off Label use of CGM in a Pediatric Patient with Type 1 Diabetes Mellitus Under the Age of 2
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HRP0092P3-53

A Case of Congenital Hyperinsulinism due to ABCC8 Mutation: A Challenge to Diagnosis, Management, and Treatment
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HRP0092P3-54

Relationship Between Chloride Infusion and Base Excess in Initial Treatment of Pediatric Diabetic Ketoacidosis
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HRP0092P3-55

The Role of Patient Adherence to Insulin Pump Therapy with Long-Term Treatment of Type 1 Diabetes
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HRP0092P3-56

Long-Term Honeymoon Period in Type 1 Diabetes: True Diagnosis MODY5; New Mutation of HNF1B
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HRP0092P3-57

Prevalence of Celiac Disease (CD) and Autoimmune Thyroid Dysfunction (AITD) in Indian Children with Type 1 Diabetes
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HRP0092P3-61

The Effect of Fibroblast Growth Factor 23 on Serum Phosphorus Level in Children with Diabetic Ketoacidosis
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HRP0092P3-62

What Does the Insulin Pump Change in Children with Type 1 Diabetes? One-Year Clinical Follow-Up
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HRP0092P3-63

Severe Heart Disease can Cause Diabetes Mellitus Even in Younger Age: Case Reports of Two Japanese Adolescent Boys
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HRP0092P3-64

De Novo Mutation of ABCC8 Gene in a Child with MODY Developed at 25 Months of Age
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HRP0092P3-65

Insulin-Induced Oedema in a Child with Newly Diagnosed Diabetes Mellitus
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HRP0092P3-67

What has Changed in Type 1 Diabetes Mellitus Cases in the Last Eight Years? A Single Center Experience
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HRP0092P3-68

Seasonal Variation and Epidemiological Parameters in Children from Western Greece with Type 1 Diabetes Mellitus (T1DM)
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HRP0092P3-69

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
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HRP0092P3-70

Indicators of Caries Risk in Children with Type 1 Diabetes Mellitus
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HRP0092P3-71

Vitamin D Status in Egyptian Children with Newly-Diagnosed Type 1 Diabetes and its Relation to Autoimmune Destruction of Pancreatic Beta Cells
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HRP0092P3-72

Hematologic Indices Indicating Platelets Activity in Children with Type 1 Diabetes
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HRP0092P3-73

The Prevalence of Hypertension and its Relationship to Glycemic Control in Children with Type 1 Diabetes Mellitus
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HRP0092P3-74

Does Metformin Therapy Prolong the Honeymoon Period in Obese Adolescent with Hybrid Diabetes?
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HRP0092P3-76

Extra Attention to be Paid When Looking After Boys with Type 1 Diabetes Mellitus in Oman
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HRP0092P3-77

Factors Affecting the Preservation of C-Peptide Secretion in Egyptian Children with Type 1 Diabetes
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HRP0092P3-78

Prevalence of Fatty Liver in Children with Type 1 Diabetes Mellitus Attending Diabetes Clinic of Alexandria University Children's Hospital
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HRP0092P3-80

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
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HRP0092P3-82

Assessment of Testicular Volume by Ultrasound in Children and Adolescents with Type 1 Diabetes
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HRP0092P3-83

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?
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HRP0092P3-84

A Low-Carbohydrate Diet Improves Metabolic Control in a Type 1 Diabetic Child Without Side Effects
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HRP0092P3-86

Clinical Profile of Paediatric Patients with type 1 Diabetes Mellitus at a Tertiary Health Care Center in the Oriental Region of Northeastern Morocco
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HRP0092P3-87

Comprehensive Analysis of HLA System Class II DRB1 in Children with Insulin Dependent Diabetes Mellitus in the North Azerbaijan and Iranian Azerbaijan
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HRP0092P3-88

A Case of Type 2 Diabetic Adolescent With Sleep Apnea who was Successfully Stopped Metformin After Adenotonsillectomy
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HRP0092P3-89

A Mitophagic Response to iron Overload-Induced Oxidative Damage Associated with the PINK1/Parkin Pathway in Pancreatic Beta Cells
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HRP0092P3-91

Association of Type 1 Diabetes and Celiac Disease In Child
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HRP0092P3-92

Case of Family Neonatal Diabetes with KCNJ11 Gene Mutation: Dynamics Monitoring
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HRP0092P3-95

Changes in the Microbiome of Pre-Type 1 Diabetic Children
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HRP0092P3-96

Assessment of Cardiac Function in Obese Children and Adolescents with Metabolic Syndrome
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HRP0092P3-97

Metabolic Syndrome in Adults with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
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HRP0092P3-98

High Allostatic Load in Children with Excess of Weight
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HRP0092P3-99

"Influence of Eating Habits, Sleep Patterns and Physical Activity on Anthropometric Variables and Body Composition in Children with Obesity"
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HRP0092P3-100

An Infant with Severe Hypertriglyceridemia: Acute and Long-Term Management in the Paediatric Population
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HRP0092P3-101

BigO: The use of New Technologies for the Management of Childhood Obesity  A Clinical Pilot Study
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HRP0092P3-102

Obesity and Insulin Resistance: Differences Between Pubertal and Prepubertal Children
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HRP0092P3-103

Relationship Between 25-Hydroxyvitamin D with Adiposity Assessed by Body Mass Index, Serum Glucose and Lipids Levels in Korea: A Cross-Sectional Analysis
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HRP0092P3-104

Treating Paediatric Morbid Obesity using the Multidisciplinary Intensive Inpatient Approach
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HRP0092P3-106

Phenotypic and Genotypic Properties of Children with Suspicion of Monogenic Obesity
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HRP0092P3-107

Relation of Serum 25 Hydroxy-Vitamin Levels D3 with Body-Mass Index in Pediatric Patients
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HRP0092P3-108

Vitamin B12 Levels in Children After Metformin Treatment
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HRP0092P3-109

Follow-Up Evaluation of Clinical Markers and Inflammatory, Biochemical and Hormonal Profiles in Children with Bodyweight Problems
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HRP0092P3-110

Gastroduodenopathies in Obese Young People
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HRP0092P3-111

Seven Methods of Indicating Childhood Metabolic Syndrome
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HRP0092P3-113

Severe Hypernatremia Revealing A Rohhad-Net Syndrome
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HRP0092P3-114

Rare Case of Acquired Generalized Lipodystrophy in A 14-Year Old Patient
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HRP0092P3-115

Gender-Based Differences in the Clustering of Metabolic Syndrome Factors in Children and Adolescents
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HRP0092P3-116

Fat Mass Index and Fat-free Mass Index Percentiles in Healthy Spanish Adolescents
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HRP0092P3-117

Comparison of Different Criteria for the Definition of Insulin Resistance and Its Relation with Metabolic Risk in Overweight and Obese Adolescents
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HRP0092P3-118

Somatostatine Analogue in Hypothalamic Obesity
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HRP0092P3-119

ESPE 2019. Physical Activity, Food and Metabolic Risk in Children and Adolescents
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HRP0092P3-120

Toward a Simple Marker of Hepato-Visceral Adiposity and Insulin Resistance:The Z-Score Change from Weight-at-Birth to BMI-in-Childhood
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HRP0092P3-121

Associations Between Lipid Parameters and Insulin Resistance in Obese Adolescents
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HRP0092P3-122

The Characteristic of Thyroid Status in Overweight and Obese Young People with Insulin Resistance
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HRP0092P3-123

Validity of Non-High-Density Lipoprotein Cholesterol for Detecting Dyslipidemia Among Korean Adolescents
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HRP0092P3-124

Early Onset Monogenic Obesity: Two Cases with Homozygous Mutation in Lepr Gene
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HRP0092P3-125

Fasting C-Peptide: A Useful Tool for Diagnosis of Type II Diabetes Mellitus in Overweight / Obese Adolescents Living in a Poor Resources Setting
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HRP0092P3-126

Metabolic Risk Assessment in Obese Children Using Hypertriglyceridemic Waist (HTGW) Phenotype. Can it be a Useful Screening Marker?
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HRP0092P3-128

Lipid and Glucose Profiles in Obese Algerian Children and Adolescents
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HRP0092P3-130

Acanthosis Nigricans as a Presentation of Severe Insulin Resistance in Obese Children
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HRP0092P3-132

Recurrent Apnea in a Boy Suffering from Congenital Hyperinsulinism in the Course of Diazoxide Treatment
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HRP0092P3-133

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
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HRP0092P3-134

Persistant Hypoglycemia in Children: Hyperinsulinemia
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HRP0092P3-137

Case Report: A neonate with Prolonged Hypoglycemia
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HRP0092P3-138

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
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HRP0092P3-139

Responses to Growth Hormone (GH) Therapy in Children with Short Stature with Normal GH Secretion and Slow Growth Velocity
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HRP0092P3-140

Assessment of Body Composition of Children with Short Stature on Growth Hormone Therapy and its Relation to Serum IGF-1
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HRP0092P3-141

Treatment Outcome of Growth Hormone in Turner Syndrome Children
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HRP0092P3-144

A Case of Paediatric GH-secreting Pituitary Adenoma Apoplexy
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HRP0092P3-146

Growth Hormone Deficiency after Radiation Therapy for Brain Tumor How to Manage?
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HRP0092P3-150

Features of Somatropin Replacement Therapy in a Patient with Floating Harbor Syndrome
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HRP0092P3-152

Linear Growth of Infants with Neonatal and Early Infantile Meningitis
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HRP0092P3-153

Prevalence of Thyroid Dysfunction and Associated Autoimmune Disorders in Young Children with Down Syndrome (DS); A Cohort Study.
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HRP0092P3-155

Turners Syndrome - Clinical Presentation, Genetics, Investigation and Management: A 10-Year Review
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HRP0092P3-156

Growth Status of Children and Adolescent Born Full Term Small-for-Gestational-Age in Korea: Data from the KNHANES-V (2010-2011)
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HRP0092P3-157

Bardet-Biedl Syndrome: A Case Series
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HRP0092P3-158

A Novel Variant of KAT6B Caused Say-Barber-Biesecker-Young-Simpson Syndrome
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HRP0092P3-159

Three Cases with Familial Short Stature: Leri-Weill Syndrome
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HRP0092P3-160

Thyroid Dysfunction in the First Year of Life in Infants with Down syndrome: Linear Growth Over 4 Years
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HRP0092P3-161

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
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HRP0092P3-163

Endocrinological Evaluation of Male Patient with Floating-Harbor Syndrome case Report
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HRP0092P3-164

Longitudinal Evaluation of Audiological Pattern in Turner Syndrome
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HRP0092P3-165

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
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HRP0092P3-166

Growth Hormone Treatment and Puberty in Patient with Pallister-Hall Syndrome
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HRP0092P3-167

Bloom Syndrome in 7-Year-Old Girl Diagnosed with Short Stature
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HRP0092P3-168

Efficacy of Growth Hormone Treatment in a Patient with Chronic Granulomatous Disease, who Developed Acute Myeloid Leukemia after Bone Marrow Transplantation
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HRP0092P3-169

Schaaf-Yang Syndrome:Three Cases Report of MAGEL2 Variation and Literature Review
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HRP0092P3-170

Reevaluation of Congenital Growth Hormone Deficiency in Adulthood
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HRP0092P3-172

Pure Gonadal Dysgenesis with Partial Testicular Development Associated with Turner Syndrome with SRY
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HRP0092P3-173

A Case of WiedemannSteiner Syndrome with Central Precocious Puberty
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HRP0092P3-174

Population Prevalence of Down's Syndrome and Cardiac Complications in South Korea: Based on National Health Insurance Service (NHIS)
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HRP0092P3-175

McCune Albright Syndrome: Two Cases with Different Clinical Courses
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HRP0092P3-178

Long-Term Effect of Growth Hormone Treatment on the Onset and Progression of Scoliosis in Children with Prader-Willi Syndrome
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HRP0092P3-179

Clinical and Molecular Characteristics of Pediatric Patients with Multiple Endocrine Neoplasia (MEN)
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HRP0092P3-180

APECED Syndrome in Childhood: Rare Clinical Presentations to Keep in Mind
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HRP0092P3-181

Phenotype and Clinical Course in Three Individuals with Multiple Endocrine Neoplasia Type 2A due to a RET Gene Mutation
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HRP0092P3-182

Two Siblings Case with Diagnosis of Autoimmune Polyglandular Syndrome Type 1
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HRP0092P3-183

High Demand for Collaborative Work Between Paediatric Endocrinologists in Arab Countries
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HRP0092P3-184

Eosinophilic Ascites: A Rare Complication of Autoimmune Polyendocrinopathy
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HRP0092P3-185

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
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HRP0092P3-186

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
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HRP0092P3-187

Difficulties in Hypothyroidism and Diabetes Treatment in Patient with GATA6 Gene Mutation case Report
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HRP0092P3-188

Endocrinopathies and Linear Growth in Adolescents with β-Thalassemia Intermedia in Relation to Liver Iron Content
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HRP0092P3-189

Bardet-Biedl Syndrome: Not Only what but also how Matters?
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HRP0092P3-190

Structural Pituitary Abnormality and Dysfunction Associated with Charge Syndrome
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HRP0092P3-191

Hormone-Secreting Pituitary Adenomas in Children and Adolescents
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HRP0092P3-192

Rohhad Syndrome: Report of 2 Rare Cases From Crete-Greece
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HRP0092P3-194

Coincidental Central Precocious Puberty and Wilms Tumor
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HRP0092P3-196

Precocious Pseudo-Puberty Presenting with Bilateral Ovarian Involvement and Progressing to Juvenile Granulosa Cell Tumor in a 2-Year-Old Girl
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HRP0092P3-197

Central Precocious Puberty in a boy with Prader-Willi Syndromeduring Growth Hormone Replacement Therapy
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HRP0092P3-198

A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation
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HRP0092P3-199

Prolactinomas in a Pediatric Population
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HRP0092P3-200

Extreme Short Stature and Neurological Impairment in a 17-Year-Old Male with Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation
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HRP0092P3-202

A Case Of Syndromic Hypopituitarism
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HRP0092P3-203

Anapylaxis Secondary to Gonadotrophin Releasing Hormone Agonist used for Precocious Puberty, Two Case Reports
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HRP0092P3-205

Childhood Craniopharyngioma: A Single Centre Experience
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HRP0092P3-206

Unusual Cause of Hypopituitarism: A Niemann Pick Disease
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HRP0092P3-207

Precocious Puberty and Primary Hypothyroidism in a 6 Years and 10 Months Girl with Pituitary Macro Adenoma and Dextral Ovarian Cyst
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HRP0092P3-209

Pituitary Hyperplasia as a Complication of Severe Hypothyroidism due to Hashimoto's Thyroiditis Could Impair Pituitary Function
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HRP0092P3-210

Homozygosity for Proopiomelanocortin (POMC) Mutation in a Palestininan Child
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HRP0092P3-211

Peculiarities of Clinical Options for Delaying Sexual Aging in Boys-Adolescents
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HRP0092P3-212

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)
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HRP0092P3-213

Mitochondrial Encephalomyopathy with Acidosis and Stroke-Like Episodes in A Vietnamese Child: Clinical, Radiological and Molecular Genetic Analysis
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HRP0092P3-214

Central Precocious Puberty in a 2 Year-Old with No Sinister Cause
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HRP0092P3-215

MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty
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HRP0092P3-216

Family Central Early Puberty about Three Sisters
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HRP0092P3-217

Clinical and Molecular Spectrum of Patients with Disorders of Sex Development: A Single Center Experience
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HRP0092P3-219

Final Adult Height in SRY-Negative 46,XX Ovotesticular Differences of Sex Development Individuals
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HRP0092P3-220

A Rare Cause of SRY (-) 46, XX DSD: Aromatase Deficiency
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HRP0092P3-221

Gonadal Dysgenesis, 46 XY About 5 Familial Cases
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HRP0092P3-223

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
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HRP0092P3-224

Clinical and Laboratory Characteristics of Different Various Types of Gonadal Dysgenesis in Girls with Hypergonadotropic Hypogonadism
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HRP0092P3-225

Evaluation of the Role of Fetuin A in Pathophysiology of Polycystic Ovarian Syndrome in Adolescents
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HRP0092P3-226

Rare Cause of 46,XY Sexual Development Disorder: 17β-Hydroxysteroid Dehydrogenase Type 3 Deficiency
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HRP0092P3-227

Persistent Elevation of Gonadotropins in a Girl with Aromatase Deficiency Despite Adequate Estradiol Supplementation- A Case for Reset Hypothalamic-Gonadal Axis
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HRP0092P3-229

Primary Amenorrhea Revealing Leydig Cell Hypoplasia
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HRP0092P3-230

Novel Heterozygous Mutation in Wilms Tumor 1 Gene in Patient with Mixed Gonadal Dysgenesis
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HRP0092P3-231

Falsely Elevated Serum Sex Steroid Hormones in a Girl with Premature Adrenarche
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HRP0092P3-232

NR5A1 Gene Mutation: Variable Phenotypes, New Variants, Different Outcomes
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HRP0092P3-233

Early Embryonic Testicular Regression Syndrome Presenting with Female External Genitalia
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HRP0092P3-234

Diagnostic Dilemma in a 46 XY Female
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HRP0092P3-235

Leydig Cell Hypoplasia in Three Siblings in the Same Family
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HRP0092P3-236

Klinefelter Syndrome Presenting with Learning Disabilities: Case Reports
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HRP0092P3-237

Gender Self-Identification and Intra-Family Relations in Children with Disorders of Sex Development
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HRP0092P3-238

Bilateral Testicular Atrophy and Normal Inhibin B level: A Paradoxal Clinical Finding For A Rare Biochemical Cause !
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HRP0092P3-239

Normosmic Hypogonadotropic Hypogonadism: An Intrafamiliar Case
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HRP0092P3-242

Clinical and Laboratory Characteristics of Patients with Different Variants of Gonadal Dysgenesis
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HRP0092P3-243

Etiologic Classification of 46, XY Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results
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HRP0092P3-244

Four-Year Experience of a New Referral Center for Gender Non-Conforming Children and Adolescents in North-East of Italy
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HRP0092P3-245

Ovarian Insufficiency: The Hidden Uterus
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HRP0092P3-246

An Adolescent Girl Presented with Hoarseness of Voice
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HRP0092P3-247

Turner's Syndrome Mosaicism 45X/47XXX with Iron Deficiency Anemia due to Menometrorrhagia
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HRP0092P3-248

Difficulties in Diagnosing Variable Disorders of Sexual Development
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HRP0092P3-249

Association of Subclinical Hypothyroidism and Dyslipidemia in Children and Adolescents
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HRP0092P3-250

Evaluation of Clinical, Demographic Data and Treatment Results of Cases with Graves' Disease
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HRP0092P3-251

A Case of Graves Disease with Negative Thyrotropin Stimulating Antibodies in a Pediatric Patient with Type 1 Diabetes
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HRP0092P3-252

An Unusual Presentation of Hypothyridism: Van Wyk-Grumbach Syndrome
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HRP0092P3-253

Child Thyrotoxicosis Syndrome: Structure and Characteristics
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HRP0092P3-254

Encephalitis Associated with Autoimmune Thyroiditis: A Rare Cause of Encephalopathy In Children
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HRP0092P3-255

Association of BMI Z-Score and Subclinical Hypothyroidism in Children and Adolescents
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HRP0092P3-256

Pseudoprecocious Puberty in a Girl with Untreated Acquired Hypothyroidism
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HRP0092P3-257

Bilateral Hip Pain as First Symptomatic Expression of Severe Primary Hypothyroidism
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HRP0092P3-258

The Challenge to Treat Neonatal Autoimmune Hyperthyroidism in a Small Preterm
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HRP0092P3-259

Graves' Disease in a 3 Year-Old Patient with Agranulocytosis due to Methimazole
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HRP0092P3-260

Hashimoto's Thyroiditis in Children: Case Series Report of Three Patients
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HRP0092P3-261

Mutation of RET Gene Causes Multiple Endocrine Neoplasia Type 2B in an Adolescent: Report of One Case and Literature Review
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HRP0092P3-262

A 12 Year Old Boy with Multifocal Papillary Thyroid Carcinoma
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HRP0092P3-263

Papillary Thyroid Cancer in Children: Single Center Results
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HRP0092P3-266

A Novel Mutation of INSR Gene in a Child with Type A Insulin Resistance
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HRP0092P3-267

Indexes of Adiposity and Body Composition in the Prediction of Metabolic Syndrome in Obese Children and Adolescents: Which is the Best
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HRP0092P3-268

Clinical, Laboratory and Radiological Assessment of Obese and Non-Obese Girls Evaluated for Early Puberty
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HRP0092P3-269

IGSF1 Mutation: Treatment in the Absence of Symptoms?
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HRP0092P3-270

A Real World, Clinical Experience of Burosumab Therapy in a Cohort of Children with X-Linked Hypophosphataemia
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HRP0092P3-271

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
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HRP0092P3-273

Insulin Sensitivity as Homa at Start and End of HGH Treatment of Children with Congenital (C) Ighd and Mphd
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HRP0092P3-274

Role of Adiposity Indexes in the Risk of Ketoacidosis (DKA) in Children with Type 1 Diabetes (T1D) at Onset
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HRP0092P3-275

Serum Spexin is Correlated with Lipoprotein(a) and Androgens in Normal-Weight, Overweight and Obese Adolescent Females
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HRP0092P3-276

Exocrine Pancreatic Insufficiency and Vitamin K Deficiency Associated to Octreotide Therapy in Congenital Hyperinsulinism: An Under-Recognized Potential Adverse Effect
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HRP0092P3-277

The Role of Urine AVP in the Diagnostic Pathway of Polyuria and Polydipsia Syndrome
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HRP0092P3-278

New Mutation of Gnas in a 2 Year Old Oncological Patient
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HRP0092P3-279

Relation between Levels of Atymullerian Hormone and Inhibin B and Spontaneous Puberty in Patients with Turner Syndrome  Preliminary Results
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HRP0092P3-280

Short, but Daily and Controlled Physical Activity of Children with Obesity has a Positive Effect on The Irisin and Chemerin Levels
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HRP0092P3-283

Comparison of Densitometric Aspects during the Transition Period in Patients with Congenital and Acquired Pituitary Deficiency: First Argentine Experience
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HRP0092P3-284

Demographic, clinical and Biochemical Characteristics of Pediatric Obesity: Interim Analysis of a Larger Prospective Study
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HRP0092P3-285

Mental Health of Both Child and Parents Play a Larger Role in Health Related Quality of Life of Obese and Overweight Children
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HRP0092P3-286

Alterations in Ambulatory Blood Pressure in Adolescents with Obesity
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HRP0092P3-287

Should Wereviewclinical Criteria to Diagnose SHOX Gene Mutations?
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HRP0092P3-288

Circulating Chemerin may be Associated with Early Vascular Pathology in Obese Children without Overt Arterial Hypertension  Preliminary Results
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HRP0092P3-289

Quality of Life of Patients with Type 1 Diabetes
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HRP0092P3-290

Etiologies and Clinical Patterns of Hypopituitarism in Sudanese Children
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HRP0092P3-291

Rare Causes for Paediatric Virilizing Tumors
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HRP0092P3-293

Clinical Evolution of a Patient with Isolated Growth Hormone Deficiency Type IA Treated with rIGF1 for 5 Years After The Development of GH-antibodies
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HRP0092P3-294

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
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HRP0092P3-296

Neonatal Severe Hyperparathyroidism - Using Genetics to Determine Treatment
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HRP0092P3-297

Liver Transplantation in Saudi Homozygous Familial Hypercholesterolemia Patients
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HRP0092P3-298

Mitchell-Riley Syndrome, A Report of Novel Mutation in a Palestinian Family Resulting in Neonatal Diabetes
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HRP0092P3-299

Review of Neonatal Cortisol Evaluation between 2012-2018 in a Single Centre: Trends, Outcomes and Associations
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HRP0092P3-300

Height and Upper/Lower Body Ratio in Turner Syndrome Adolescents in Indonesia; Is There any Significant Difference Based on Karyotype?
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HRP0092P3-301

A Novel Heterozygous Mutation in The SLC5A2 Gene Causing Mild Failure to Thrive and Subclinical Hypoglycemia in a 2-year Old Girl
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HRP0092P3-302

Cognitive and Learning Performance of Children and Adolescents Cancer Survivors
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HRP0092P3-303

Hirsutism in Children: Pitfalls and Diagnostic Challenges
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HRP0092P3-304

Congenital Craniopharyngioma - A Rare Case of Congenital Hypopituitarism
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HRP0092P3-305

Combined Surgical and Medical Treatment in an Adolescent with Severe Gynecomastia Due to Excessive Estradiol Secretion: A Case Report
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HRP0092P3-306

Improvement of Metabolic Control in Children with Type1 Diabetes Using Continuous Glucose Monitoring Devices
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HRP0092P3-307

Autoimmune Thyroiditis in Beta Thalassemia Major after the Hematopoietic Stem Cell Transplantation - Case Report
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HRP0092P3-308

Grave's Disease: What Place in the Child's Hyperthyroidism?
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HRP0092P3-309

Vitamin D Status Among Children and Adolescents in an Egyptian Cohort: Can we Predict Vitamin D Deficiency?
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HRP0092P3-310

Case Report: Primary Hyperparathyroidism Presenting as a Brown Tumor of Mandible in an Adolescent Girl - An Unusual Presentation with Challenges and Outcome
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HRP0092P3-311

Serum Calcium, 25(OH) Vitamin D and Bone Alkaline Phosphatase in Children with Epilepsy Receiving Antiepileptic Drugs in University of Port Harcourt Teaching Hospital
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HRP0092P3-314

Case Report: Hyperglicemic Iperosmolar State in a Obese Prepubertal Girl with Newly Diagnosis of Type 2 Diabetes
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HRP0092P3-315

Associations between Pituitary Abnormalities and Treatment Response in Children with Growth Hormone Deficiency. First Multicenter Study in Portugal
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HRP0092P3-316

Epidemiological and Socioeconomic CHANGES in the Child Population from Debut DM1 in this 21st Century
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HRP0092P3-317

Body Mass Index and Incident Type 1 Diabetes in Children from Lesser Poland Over an 11 Year Observation Period
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HRP0092P3-318

Novel Mutation in HNF4-Alpha Gene and Reclassification of Diabetes in a Family
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HRP0092P3-319

Systemic Lupus Erythematosus, Celiac and Hypothyroidism Complicating Type 1 Diabetes: A Rare Tetrad
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HRP0092P3-320

EpiPEG-PreMeb Study: Chemerina Plasmatic and Metabolic Syndrome Relation at SGA Childrens
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HRP0092P3-321

Hydrometrocolpos Due to Congenital Adrenal Hyperplasia  A Rare Cause of Bladder Outflow Tract Obstruction in a Female Child
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HRP0092P3-322

Bartter Syndrome Complicated with Growth Hormone Deficiency Due to a Suprasellar Arachnoid Cyst
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HRP0092P3-324

Hypoglycemia in a Patient with Turner Syndrome and Kabuki Make-Up
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HRP0092P3-325

45X/47XXX Mosaicism and Progressive Puberty
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HRP0092P3-326

Vitamin D and Type 1 Diabetes Mellitus in Children
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HRP0092P3-327

Severe Hypercalcaemia After Years on The Ketogenic Diet: A Novel Case Report
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HRP0092P3-328

Estrogen Production by Sertoli Cell Tumor in Unusual Case of Testicular Feminization Syndrome
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HRP0092P3-329

Dysphagia and Dyspnea by Lingual Thyroid Mass in a Young Child: What To Do?
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HRP0092P3-330

Van-Wyk Grumbach Syndrome Associated with Trisomy 21: A Case Report
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HRP0092P3-331

Fahr Syndrome in Young Boy with Hypoparathyroidism
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HRP0092P3-332

Thyroid Cancer in a Child with Graves's Disease
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HRP0092P3-333

Influence of Nocturnal Hypoglycemia on School Performance of Teens with DM Type1
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ESPE Abstracts

58th Annual ESPE (ESPE 2019)

EPosters

BiosciAbstracts