ePosters

HRP0089RFC1.1

The Relative Contributions of Genetic and Environmental Factors on Cortisol Metabolism at Pre-, Mid- and Post-Pubertal Ages
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HRP0089RFC1.2

Changes in CYP19A1 and CYP3A4 Activities due to Population Genetic Variations in Human P450 Oxidoreductase
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HRP0089RFC1.3

Sphingosine-1-Phosphate Lyase (SGPL1) Deficiency is Associated with Mitochondrial Dysfunction
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HRP0089RFC1.4

Mass Spectrometry-Based Assessment of Childhood Androgen Excess in 487 Consecutive Patients Over 5 Years
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HRP0089RFC1.5

Quantitative Urinary GC-MS Based Steroid Analysis for Treatment Monitoring of Adolescents and Young Adults with Autoimmune Primary Adrenal Insufficiency
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HRP0089RFC1.6

A Laboratory Harmonization Strategy for Steroid Hormone Profiling by MoM-Transformed, Normalized Reference Ranges Independent of Age, Sex and Units
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HRP0089RFC2.1

High-Resolution MRI Imaging of Bone-Muscle-Fat in Glucocorticoid Treated Boys with Duchenne Muscular Dystrophy: Results from the ScOT-DMD Study
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HRP0089RFC2.2

S-25OHD is Associated with Hand Grip Strength and Myopathy at Five Years in Girls: An Odense Child Cohort Study
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HRP0089RFC2.3

Measured Free 25-Hydroxyvitamin D in Healthy Children and Relationship to Total 25-Hydroxyvitamin D, Calculated Free 25-Hydroxyvitamin D and Vitamin D Binding Protein
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HRP0089RFC2.4

Novel Severe Skeletal Dysplasia with Under-Mineralisation Associated with Reduced In Utero Calcium Transport and TRPV6 Compound Heterozygous Variants
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HRP0089RFC2.5

Identification of Characteristic Neurological Complications in Infants with Achondroplasia by Routine MRI Screening
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HRP0089RFC2.6

The Novel R211Q POP1 Homozygous Mutation Causes Severe Short Stature But Uniquely Only Subtle Skeletal Dysplasia
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HRP0089RFC3.2

Personalized and Predictive Medicine for Pediatric Diabetes Through a Genetic Test Using Next Generation Sequencing
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HRP0089RFC3.3

Significant Prevalence of Severe Monogenic Immune Defects Among Children with Type 1 Diabetes and Low T1D-Genetic Risk Score
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HRP0089RFC3.4

Functional Characterization of a Novel KLF11 Mutation Identified in a Family with Autoantibody-Negative Type 1 Diabetes
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HRP0089RFC3.5

Recent Secular Change in Pre- and Postnatal Growth and Adiposity in Infants of Mothers with Gestational Diabetes
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HRP0089RFC3.6

Treatment Adherence and Weight Loss are Key Predictors of HbA1c One Year after Diagnosis of Childhood Type 2 Diabetes in UK
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HRP0089RFC4.2

Data Mining and Computational Analysis of Human Growth Hormone Gene (GH1) Sequence in Normal Population to Identify Potential Variants with Disease-Causing Effects
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HRP0089RFC4.4

A Longitudinal Study on miRNAs Circulating Levels in a Cohort of SGA and AGA Subjects, Evaluated During Childhood and Young Adulthood
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HRP0089RFC4.5

12-Month Effects of Once-Weekly and Twice-Monthly Administration of Hybrid Fc-Fused Human Growth Hormone, GX-H9, Treatment in Pediatric with GHD Deficiency
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HRP0089RFC4.6

Effect of 2 Years of Growth Hormone Treatment on Glucose Tolerance in Adults with Prader-Willi Syndrome
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HRP0089RFC5.1

Serum Levels of the Soluble Receptor for Advanced Glycation End Products are Reduced in Children with Hashimoto's Thyroiditis
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HRP0089RFC5.2

Analysis of Chosen Polymorphisms rs7138803 A/G - FAIM2, rs7093069 C/T - IL-2RA, rs5742909 C/T - CTLA-4 in Pathogenesis of Hashimoto's Thyroiditis in Children
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HRP0089RFC5.3

Incidence and Treatment Outcome of Childhood Thyrotoxicosis
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HRP0089RFC5.4

The Value of Cytological, Histological and US Examination to Determine of Management Children with Nodular Goiter
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HRP0089RFC5.5

Evidence for a Founder Effect in Multiple Endocrine Neoplasia 2
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HRP0089RFC5.6

DUOX2 Deficiency in Quebec: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism
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HRP0089RFC6.2

IGF-I at Four Months Associates to Visceral and Subcutaneous Adipose Tissue at 7 Years of Age
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HRP0089RFC6.3

Effect of the Melanocortin-4 Receptor Agonist, Setmelanotide, on Obesity and Hyperphagia in Individuals Affected by Bardet-Biedl Syndrome
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HRP0089RFC6.4

Functionality and Phenotypic Characteristics of Mutations in the Human Leptin Receptor
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HRP0089RFC6.5

High-Throughput Untargeted Plasma Metabolomics Unravels Gender Dimorphic Metabolic Trajectories in Naturally Conceived and ICSI Prepubertal Children
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HRP0089RFC7.1

Next Generation Sequencing Results in 142 Patients with Congenital Hyperinsulinism
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HRP0089RFC7.2

Outcomes of a Quality Improvement Project Integrating Continuous Glucose Monitoring Systems into the Routine Management of Neonatal Hypoglycaemia
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HRP0089RFC7.3

Central Venous Cathether-Associated Thrombosis in Children with Congenital Hyperinsulinism
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HRP0089RFC7.4

Expression of MIR-576-5p in Umbilical Cord as a Novel Biomarker for the Identification of Catch-up Growth in Small-For-Gestational-Age Infants
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HRP0089RFC7.5

Alteration of Renal Corticosteroid Signaling Pathways in Preterm Infants: Neonatal Adaptation and Developmental Programming of Hypertension
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HRP0089RFC7.6

Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases
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HRP0089RFC8.1

Male Fertility Genes Located in Y-Chromosomal Regions Display Differential mRNA Profiles in Response to GnRH Treatment of Cryptorchidism-Dependent Infertility
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HRP0089RFC8.2

High Mobility Group Box 1 (HMGB1) is Increased in Adolescents with Polycystic Ovarian Syndrome (PCOS) and Decreases after Treatment with Myo-Inositol in Combination with [alpha]-Lipoic Acid (MYO+ALA)
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HRP0089RFC8.3

Pharmacological Treatment of Adolescent Polycystic Ovary Syndrome (PCOS) According to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS
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HRP0089RFC8.4

Establishing Age, Sex, and Method Related Reference Ranges for Anogenital Distance - a Marker of In Utero Androgen Action
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HRP0089RFC8.5

Latest Progress in Tissue Engineered Urethral Regeneration: From Rabbit to Dog, a Step from Human Clinical Trial for Surgical Treatment of VSD (Variation of Sex Development)
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HRP0089RFC9.2

Novel Variant in GNRHR Gene Regulatory Region in a Pedigree with Maternally Inherited Precocious Puberty
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HRP0089RFC9.3

What is the Best Parameter to Decide the Initial Dose of Depot Leuprolide Acetate in Girls with Idiopathic Central Precocious Puberty?
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HRP0089RFC9.4

REplacement of MAle mini-Puberty in Neonates and Children with Micropenis and Cryptorchidism due to Hypogonadotropic Hypogonadism: Results of the 'REMAP' Study ISRCTN13007297
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HRP0089RFC9.5

Non-Isolated Central Precocious Puberty: Prevalence of Brain Lesions and Other Associated Disorders
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HRP0089RFC9.6

Can Neuroimaging Predict Endocrine Morbidity in Congenital Hypothalamo-Pituitary (H-P) Disorders?
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HRP0089RFC10.1

Patients with GH Insensitivity and IGF-1 Resistance Harbour Copy Number Variants Causing a Silver-Russell-Like Phenotype
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HRP0089RFC10.2

Non-Inferiority Clinical Trial on Gonadotropinversus Pulsatile Gonadotropin-Releasing Hormone Infusion Therapy in Male Adolescent Patient Withcongenital Hypogonadotropic Hypogonadism
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HRP0089RFC10.3

Developmental Regulation of Obestatin and Adropin in Prader-Willi Syndrome and Non-Syndromic Obesity: Associations with Weight, BMI-z, HOMA-IR, and Lipid Profile
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HRP0089RFC10.4

Comparative Analysis between Immunoassay and Tandem Mass Spectrometry for Androgens before and after Human Recombinant Gonadotrophin in Children with Genital Ambiguity and 46,XY Karyotype
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HRP0089RFC10.6

Effect of the Current Treatment of X-Linked Hypophosphatemia During Growth on the Development of Osteoarticular Lesions in the Hyp Mouse Model
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HRP0089RFC11.1

Diagnosis and Management of Pseudohypoparathyroidism and Related Disorders: First International Consensus Statement
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HRP0089RFC11.2

Nationwide Hypophosphatemic Rickets Study
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HRP0089RFC11.3

Increased Levels of Bone Formation and Resorption Markers in Patients with Hypophosphatemic Rickets
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HRP0089RFC11.4

A New Form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency Caused By Abolished Store-Operated Ca2+ Entry
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HRP0089RFC11.5

The Determinants of Skeletal Fragility in Children with Type 1 Diabetes Mellitus
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HRP0089RFC11.6

Reference Values of Automated Bone Age and Bone Health Index for Mexican Children and Adolescents
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HRP0089RFC12.1

Use of Acid-Suppressivemedications During Infancy and Early Childhood and Its Association with Type 1 Diabetes
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HRP0089RFC12.2

Bone Mineral Density is Increased in 276 Danish Children and Adolescents with Type-1-Diabetes
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HRP0089RFC12.3

Barriers and Sources of Support for the Performance of Physical Activity in Pediatric Type 1 Diabetes
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HRP0089RFC12.4

Use of Telemonitoring Via a Mobile Device App Reduces HbA1c in Type 1 Diabetic Children and Adolescents
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HRP0089RFC12.5

Insulin Gene Promoter Methylation Status in Greek Children and Adolescents with Type 1 Diabetes
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HRP0089RFC12.6

AMGLIDIA, a Suspension of Glibenclamide for Patients with Neonatal Diabetes, Long Term Data on Efficiency and Tolerance
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HRP0089RFC13.2

Growth Outcomes and Near Adult Height of Children with Congenital GH Deficiency (GHD) due to Abnormal Pituitary Development: Data from a Prospective, Multinational Observational Study
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HRP0089RFC13.3

Circulating MKRN3, Kisspeptin and IGF-1 Levels in Girls During the Clinical Onset of Puberty
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HRP0089RFC13.4

Gain in Predicted Adult Height Using the Combination of an LHRH Analogue and an Aromatase Inhibitor in Early Maturing Girls with Compromised Growth for 2 yrs or Until the Age of 11 is Maintained and Further Improved by Aromatase Inhibitor Monotherapy: Results on Final Height of the 'GAIL' Study ISRCTN11469487
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HRP0089RFC13.5

Pubertal Voice Break: Temporal Relation of Secondary Sexual Characteristics in Healthy Boys
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HRP0089RFC13.6

Close Correlation between Salivary and Blood Steroids in Normal Boys: Salivary Testosterone Best Characterizes Male Puberty
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HRP0089RFC14.1

Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer
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HRP0089RFC14.2

British Society for Paediatric Endocrinology and Diabetes Peer Review of Specialised Paediatric Endocrinology Services in the UK - Evaluation of the Outcomes
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HRP0089RFC14.3

Dysregulated Glucose Homeostasis in Congenital Central Hypoventilation Syndrome
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HRP0089RFC14.4

A Novel Germline DICER1 Mutation in a Girl with Multinodular Goiter and Ovarian Sertoli-Leydig Cell Tumor
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HRP0089RFC14.5

Natural Course of MEN Type 2B Syndrome; a Dutch Single-Center Cohort
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HRP0089RFC14.6

Identification of Epithelial Sodium Channel (ENaC) in Endometrial Pipelle Biopsy Samples
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HRP0089RFC15.2

Molecular and Clinical Analyses of Two UPD(16)mat Patients Detected by Screening of 94 Silver-Russell Syndrome Patients without Known Etiology
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HRP0089RFC15.3

Multiple Pituitary Hormone Deficiencies and Early Onset Obesity in Two Siblings with a Mutation in the MAGEL2-gene: Evidence for an Important Regulatory Function of the MAGEL2-gene in the Hypothalamic-Pituitary Hormone Pathways
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HRP0089RFC15.4

Characteristics, Effectiveness and Safety Data from Clinically Relevant Subgroups of Patients with Severeprimary IGF-I Deficiency (SPIGFD): Results from the European Increlex® Growth Forum Database (EU-IGFD) Registry
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HRP0089RFC15.5

Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths
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HRP0089RFC15.6

Latest Results from PATRO Children, a Multi-Centre, Non-Interventional Study of the Long-Term Safety and Efficacy of Omnitrope® in Children Requiring Growth Hormone Treatment
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HRP0089P1-P001

Evaluation of Long Term Metabolic Effects After Prenatal Dexamethasone Treatment in the Context of CAH - the Swedish Cohort
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HRP0089P1-P002

Obesity and Cardio-metabolic Risk Factors among Children and Adolescents with Non-Classic 21-Hydroxylase Deficiency
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HRP0089P1-P003

Cognition in Children with Congenital Adrenal Hyperplasia
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HRP0089P1-P004

Carriers of CYP21A2 Mutations have Decreased Mortality in Infectious Diseases, Anational Population Registry Study
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HRP0089P1-P005

Elevated Concentrations of Adrenal Steroid Precursors with Glucocorticoid Activity Might Prevent Addisonian Crisis in Untreated Patients with Classic Congenital Adrenal Hyperplasia
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HRP0089P1-P006

Altered DNA Methylation in Peripheral T-cells from Patients with Congenital Adrenal Hyperplasia
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HRP0089P1-P007

Birth Incidence, Age at Diagnosis, Mortality in Congenital Adrenal Hyperplasia in Korea: A Nationwide Population-based Study
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HRP0089P1-P008

Impact of Puberty on Final Height in Children and Adolescents with Congenital Adrenal Hyperplasia (CAH)
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HRP0089P1-P009

The Relationship of Baseline, Incremental and Peak Cortisol Following a Short Synacthen Test - Single-centre Analysis of Three Years' Data
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HRP0089P1-P010

The Circadian Rhythm of Cortisol Binding Globulin has Little Impact on Cortisol Exposure after Hydrocortisone Dosing
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HRP0089P1-P011

Characterizing the Steroidome in Ammniotic Fluid of Mid-gestation by LC-MS/MS
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HRP0089P1-P012

Pediatric Adrenocortical Tumors. A Single Tertiary Center Experience: Clinical, Biological and Pathologic Characteristics Analysis
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HRP0089P1-P014

Molecular Characterization of TNXA/TNXB Chimeras in CYP21A2 Gene Deletions: High Frequency of Undiagnosed Ehlers-Danlos Syndrome in Congenital Adrenal Hyperplasia Patients
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HRP0089P1-P015

New Insights into Low Dose Dexamethasone Suppression Test in Paediatric Cushing's Syndrome
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HRP0089P1-P016

Recurrent Hypoglycemia in a Preschooler Girl with Overgrowth: Isolated ACTH-Deficiency with a Novel TPIT Mutation
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HRP0089P1-P017

Biochemical, Genetic and Molecular Characterization of a Novel P399_E401Dup Mutation in P450 Oxidoreductase (POR) Altering Several Enzymatic Activities in a Patient with a 46,XX DSD Phenotype at Birth
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HRP0089P1-P018

Young Lean Women with Evidence of Both Premature Adrenarche and Pubarche Display a Metabolic, Hormonal and Psychologic Profile that is Similar to that of their Peers with Polycystic Ovary Syndrome
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HRP0089P1-P019

The Usefulness of Combined Analysis of Serum and Salivary Maximum Cortisol Response to Low-Dose ACTH Test to Define the Requirement of Hormone Replacement Treatment
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HRP0089P1-P020

High DHEAS (HD) in Girls Determines Earlier Pubertal Maturation and Mild Hyperandrogenism throughout Pubertal Development
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HRP0089P1-P021

Higher Dehydroepiandrosterone Levels in Prepubertal Children Born Very Preterm
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HRP0089P1-P022

A Large Consanguineous Family with a Mild and Transient form of Autosomal Recessive Pseudohypoaldosteronism type 1 (PHA1) Caused by a Novel Mutation in the SCNN1A Gene: Functional Studies
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HRP0089P1-P023

Associations Between Maternal and Offspring Hair Cortisol Concentrations and Child Behavioral Symptoms in Pairs of Children 18-48 Months Old and their Mothers With and Without Perinatal Mental Disorders
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HRP0089P1-P024

Gonadotropin-Dependent Pubertal Disorders are Common in Patients with Virilizing Adrenocortical Tumors in Childhood
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HRP0089P2-P001

Contribution of Direct Measurements of Steroids by Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS) in Non-classical Adrenal Hyperplasia (NCCAH)
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HRP0089P2-P002

GnRH-analogue Treatment in Children with Congenital Adrenal Hyperplasia (CAH): Data from a Multicenter CAH Registry
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HRP0089P2-P003

Glucocorticoid Replacement Regimens in the Treatment of 21-hydroxylase Deficiency Congenital Adrenal Hyperplasia: A Systematic Cochrane Review
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HRP0089P2-P004

Hydrocortisone (HC) Dose in Children with Congenital Adrenal Hyperplasia (CAH)
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HRP0089P2-P005

Perioperative Care of CAH - Incongruencies of Practices among Canadian Specialists
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HRP0089P2-P006

Analysis of Phenotypes and Genotypes in 84 Patients with 21-hydroxylase Deficiency
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HRP0089P2-P007

Miscarriages in Families with a Child with Classic Congenital Adrenal Hyperplasia and 21-Hydroxylase Deficiency (CAH)
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HRP0089P2-P011

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38 935 Infants
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HRP0089P2-P012

Autoantibodies Against 21-Hydroxylase in Prediction of Adrenal Failure in APECED Patients
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HRP0089P2-P013

A First Combination Case of 21-Hydroxilase Deficiency and CHARGE Syndrome Confirmed by Genetic Analysis
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HRP0089P2-P014

Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients
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HRP0089P2-P015

Study of Cardiovascular Risk Factors and Carotid Intima-Media Thickness in Children with Congenital Adrenal Hyperplasia
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HRP0089P2-P016

The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective Analysis
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HRP0089P2-P017

Childhood Growth Advancement in Girls with Premature Adrenarche Heralds Anabolic Effects by Adulthood
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HRP0089P2-P018

A Novel Mutation in the MC2R Gene in a Two-year-old Boy with Adrenal Insufficiency
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HRP0089P2-P019

Two Cases of Apparent Mineralocorticoid Excess due to Novel Mutations in HSD11B2 Gene
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HRP0089P2-P020

Long-term Follow-up of Safety and Disease Control for Hydrocortisone Granules Designed to give Age-appropriate Dosing with Taste Masking to Children with Adrenal Insufficiency
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HRP0089P2-P021

Borderline Peak Plasma Cortisol Following Synacthen Stimulation - Single-centre Analysis of Three Years Data
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HRP0089P2-P022

Unilateral Adrenalectomy for Primary Pigmented Nodular Adrenocortical Disease Causing Cushing Syndrome
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HRP0089P2-P023

Adrenal Crisis in Children with Adrenal Insufficiency: Prevalence and Risk Factors
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HRP0089P2-P024

The Effectiveness of a Stress-Management Intervention Program in Behavioral Parameters and Hair Cortisol Concentrations in Children with Attention Deficit Hyperactivity Disorder
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HRP0089P2-P025

Very High Dehydroepiandrosterone Sulfate (DHEAS) in Serum of an Overweight Female Adolescent without a Tumor
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HRP0089P2-P026

Early Recognition of Adrenal Insufficiency after Hematopoietic Stem Cell Transplantation During Childhood
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HRP0089P2-P027

Reference Values for Serum 17-alfa Hydroxyprogesterone and Adrenal Size in Healthy Newborns
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HRP0089P2-P028

A Rare Case of ACTH-Independent Cushing's Syndrome due to Bilateral Micronodular Adrenal Hyperplasia and Myoclonic Dystonia
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HRP0089P2-P029

Two Siblins and Three Cousins with Allgrove (4A) Syndrome in a Turkısh Family: A Novel Mutation in the 'Aladin' Gene
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HRP0089P2-P030

Ganglioneuroma Presenting as an Adrenal Incidentaloma in a 10-year-old boy-a Rare Entity
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HRP0089P2-P032

Adrenal Hypoplasia Seemingly First as a Primary Hypoaldosteronism
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HRP0089P2-P033

Quantitative Ultrasound Evaluation in a Cohort of 43 Young Adults with Classical CAH due to 21-Hydroxylase Deficiency (21OHD): Is Bone Mineral Quality Impaired?
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HRP0089P3-P002

An Extremely Rare Cause of Cushing Syndrome in Chidhood
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HRP0089P3-P003

Nelson's Syndrome after Bilateral Adrenalectomy for Cushing's Disease in Pediatric Age - Report of a Case
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HRP0089P3-P004

Basal Levels of 17-hydroxyprogesterone can Distinguish Isolated Precocious Pubarche from Non-Classical Congenital Adrenal Hyperplasia in Children: A Prospective Observational study
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HRP0089P3-P005

Age at Diagnosis and Outcome in Maghreb patients with 21-hydroxylase Deficient Congenital Adrenal Hyperplasia; Urgent need for Newborn Screening
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HRP0089P3-P006

An Adrenal Tumor Ppresenting as a Premature Pubarche in a 7 Year-old Girl
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HRP0089P3-P007

Refractory Cyclical Cushing's Disease - a Case of Multiple Pituitary Micro-adenomas in a Three Year Old Girl after 8 Years Follow up
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HRP0089P3-P008

Topical Corticosteroid-Induced Adrenal Insufficiency
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HRP0089P3-P009

Early Diagnosis of Duchenne Muscular Dystrophy in 6-Months-Old Male with Primary Adrenal Insufficiency
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HRP0089P3-P010

Lipoid Adrenal Hyperplasia Diagnosed with Severe Cholestasis in Newborn
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HRP0089P3-P011

Severe Hyponatraemia with Absence of Hyperkalaemia in a Patient with Addison's Disease
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HRP0089P3-P012

Deep Bronze Skin without Sun Exposition in a 16-Year Old Girl
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HRP0089P3-P013

Case of Primary Pigmented Nodular Adrenocortical
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HRP0089P3-P014

Two Case Report of Adrenocortical Adenoma
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HRP0089P3-P015

A Homozygous Mutation c.518T>A (p.lle173Asn) of the CYP21A2 Gene Presenting as Non-Classical Congenital Adrenal Hyperplasia (NCAH)
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HRP0089P3-P016

Adrenals and HPA Axisa; Atypical Presentation of Adrenal Insufficiency
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HRP0089P3-P017

Non-classic Congenital Adrenal Hyperplasia Causing Alleles among Adolescent Girls with PCOS - Genetical Study
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HRP0089P3-P018

Adequate Interpretation of Cortisol Levels in Children
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HRP0089P3-P019

Erythrocytosis as First Manifestation of Adrenal Mass
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HRP0089P3-P020

A Neonatal Case with Familial Glucocorticoid Deficiency Type 1 Having Adrenal Crisis in Early Period
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HRP0089P3-P021

Presenting Features, Clinical Characteristics and Follow up of Familial Isolated Glucocorticoid Deficiency (FGD) due to Mutations in MC2R and MRAP Genes
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HRP0089P3-P022

Identification of X-linked Adrenoleukodystrophy in Boys Presenting with Adrenal Insufficiency in the Absence of Adrenal Antibodies
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HRP0089P3-P023

Secondary Hyperaldosteronism in the Course of Cystic Fibrosis
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HRP0089P3-P024

The P30L Mutation in the CYP21A2 Gene in a Girl with Congenital Adrenal Hyperplasia with Hidden Salt Loosing and Central Precocious Puberty
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HRP0089P3-P025

Congenital Adrenal Hyperplasia due to a Rare Homozygous Mutation R483P in the CYP21A2 Gene and Coexisting Growth Hormone Deficiency
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HRP0089P3-P026

Rare Case of Androgen Producing Tumor in 14 Month Old Girl
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HRP0089P3-P027

Adrenocortical Tumours in Children - A Case Series
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HRP0089P3-P028

Discrete Virilization in Girls with the Classic Form of Congenital Adrenal Hyperplasia: the Importance of a Detailed Genital Examination at Birth
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HRP0089P3-P029

A New Methodology for Early Identification of Steroid Resistant Acute Graft-Versus-Host Disease Patients
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HRP0089P3-P030

Delayed Diagnosis of a Patient with Antley-Bixler Syndrome
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HRP0089P3-P404

Clinical and Biochemical Phenotype of Aldosterone Synthase Deficiency
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HRP0089P3-P414

Is the Third Time Really a Charm? The Story about Three Brothers Suffering from Adrenoleukodystrophy and about HSCT being a Chance to Stop the Unstoppable Disease
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HRP0089P1-P026

Duration of Breastfeeding and Bone Mineral Density in Childhood - A Prospective Study Among Preschool Children
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HRP0089P1-P027

Bone Health in Adolescents Born Small for Gestational Age (SGA)
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HRP0089P1-P028

Longitudinal Study of Bone Mass in Swedish Children Treated with Modified Ketogenic Diet
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HRP0089P1-P029

Fracture Epidemiology for Children in Western Australia between 2005-2015: Do We Need to be Concerned about Bone Health?
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HRP0089P1-P030

Bone Biochemistry in Children with Fractures Presenting with Suspected Non-accidental Injury
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HRP0089P1-P031

Systematic Screening Using DXA Lateral Vertebral Morphometry is Associated with a High Prevalence of Vertebral Fractures in Duchenne Muscular Dystrophy: Results from ScOT-DMD Study
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HRP0089P1-P032

Bone Mineral Density and Glycemic Control in Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0089P1-P033

Comparison of Manual and Automated Bone Age Assessment in 1285 Children and Adolescents Aged 5 to 16 Years
Direct

Abstract PDF
HRP0089P1-P034

Is Plasma C-Type Natriuretic Peptide Level Available for Typing and Diagnosis of Skeletal Dysplasia Cases?
Direct

Abstract PDF
HRP0089P1-P035

Long-term Outcomes of Osteogenesis Imperfecta in the Bisphosphonate Era
Direct

Abstract PDF
HRP0089P1-P036

Novel LRP5 Loss-of-function Mutation Causes Osteoporosis-pseudoglioma Syndrome
Direct

Abstract PDF
HRP0089P1-P037

Hypercalcaemia after Treatment with Denosumab in Children: Bisphosphonates as an Option for Therapy and/or Prevention?
Direct

Abstract PDF
HRP0089P1-P038

Disease Burden and Systemic Manifestations of HPP in Children Enrolled in the Global HPP Registry
Direct

Abstract PDF
HRP0089P1-P039

3-epi-25 Serum 25-hydroxyvitamin D3 Concentrations in Chilean Children between 5 and 8 Years
Direct

Abstract PDF
HRP0089P2-P036

Length Estimation Based on Clinical and Anthropometric Measures in Newborns
Direct

Abstract PDF
HRP0089P2-P037

Vitamin D Deficient (Nutritional) Rickets Presenting in Infancy
Direct

Abstract PDF
HRP0089P2-P038

The Effect of Vitamin D Receptor Polymorphism on Bone Mineral Density in Egyptian Patients with Beta Thalassemia Major
Direct

Abstract PDF
HRP0089P2-P039

Vitamin D in Adolescents: A Comprehensive Review of Guidelines and Recommendations
Direct

Abstract PDF
HRP0089P2-P040

X-linked Hypophosphatemia Registry - An International Prospective Patient Registry
Direct

Abstract PDF
HRP0089P2-P041

Clinical and Biological Parameters Associated to the Severity of X-linked Hypophosphatemia in Children
Direct

Abstract PDF
HRP0089P2-P042

High Fibroblast Growth Factor (FGF) 23: An Unusual Cause of Severe Osteoporosis in a Patient with Chronic Liver Disease
Direct

Abstract PDF
HRP0089P2-P043

Metabolic Syndrome in Children with X-linked Hypophosphatemic Rickets (XLHR)
Direct

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HRP0089P2-P044

High Incidence of Cranial Synostosis and Chiari Malformation in Children with X-linked Hypophosphatemic Rickets
Direct

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HRP0089P2-P045

An Unusual Case of Hypophosphatemia in a Child Affected by Di George Syndrome
Direct

Abstract PDF
HRP0089P2-P046

Novel SLC34A1 Mutation in a Girl Infant with Idiopathic Infantile Hypercalcemia
Direct

Abstract PDF
HRP0089P2-P047

A Novel Variant of SLC34A1 Gene in an Infant with Idiopathic Infantile Hypercalcemia
Direct

Abstract PDF
HRP0089P2-P048

Infantile Arterial Calcification and Subsequent Hypophosphatemia due to ENPP1 Mutation - A Case Followed through to Adulthood
Direct

Abstract PDF
HRP0089P2-P049

Pediatric Quality of Life Inventory in Children with Osteogenesis Imperfect in Dr Soetomo Hospital Surabaya
Direct

Abstract PDF
HRP0089P2-P050

Osteoporosis-pseudoglioma Syndrome (OPPG): Improvement of Osteoporosis on Biphosphonate Therapy
Direct

Abstract PDF
HRP0089P2-P052

Evaluation of Bone Mineral Density in a Cohort of Children with Growth Hormone Deficiency
Direct

Abstract PDF
HRP0089P2-P053

Follow-up on Bone Health in Children with Acute Lymphoblastic Leukemia (ALL)
Direct

Abstract PDF
HRP0089P2-P054

Effect of Pubertal Inductionn Bone Mass Accrual, in Adolescent Boys with Duchenne Muscular Dystrophy
Direct

Abstract PDF
HRP0089P2-P056

First Reported Cases of a Novel Variant of GNAS 1 Gene
Direct

Abstract PDF
HRP0089P2-P057

An Unusual Cause of Short Stature
Direct

Abstract PDF
HRP0089P2-P058

Validation of an Automated Method (BoneXpert) for the Determination of Bone Age in Paediatric Endocrinology - A Single Centre Experience
Direct

Abstract PDF
HRP0089P2-P059

Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism
Direct

Abstract PDF
HRP0089P3-P031

Growth Hormone Treatment of 2 Patients with X-linked Hypophosphatemic Rickets Caused by PHEX Mutation: Effects on Linear Growth
Direct

Abstract PDF
HRP0089P3-P032

A Novel Homozygous Mutation in the CASR Gene in a Neonate with Severe Primary Hyperparathyroidism; A Case Report
Direct

Abstract PDF
HRP0089P3-P033

A 13 Year-Old Boy Diagnosed as Osteogenesis Omperfecta with Normal Bone Mineral Density
Direct

Abstract PDF
HRP0089P3-P034

A Rare Cause of Hypercalcemia in Childhood: Hypercalcemia Associated with Parathormon-Related Peptid
Direct

Abstract PDF
HRP0089P3-P035

Our Treatment Experience with Nocturnal Continuous Enteral Calcium Infusion in a Case with Vitamin D Resistance Rickets Type II
Direct

Abstract PDF
HRP0089P3-P037

Hypophosphatemic Hypercalciuric Ricket: 3 Brothers with Dent's Disease
Direct

Abstract PDF
HRP0089P3-P039

Carbonic Anhydrase Deficiency: Three Siblings
Direct

Abstract PDF
HRP0089P3-P040

A Novel p.Gly775Glu Missense COL1A2 Mutation Causes Severe Osteogenesis Imperfecta in a Prepubertal Girl
Direct

Abstract PDF
HRP0089P3-P041

SHOX Gene Deletion Screening by FISH in Children with Short Stature and Characteristics of Patients
Direct

Abstract PDF
HRP0089P3-P042

Pseudoachondroplasia
Direct

Abstract PDF
HRP0089P3-P043

Low Level of Vitamin D in Children Increases the Risk of Bone Fractures
Direct

Abstract PDF
HRP0089P3-P044

Clinical Evaluation of Eight Patients with Parathyroid Adenoma
Direct

Abstract PDF
HRP0089P3-P045

Idiopathic Hypoparathyroidism in a 10 Year-Old Girl with Concomitant Epilepsy, Long Q-T Syndrome (LQTS), Pericarditis and Pneumonia
Direct

Abstract PDF
HRP0089P3-P047

Evaluation of Bone Mineral Density and Bone Metabolism Markers in Children Diagnosed as Celiac Disease
Direct

Abstract PDF
HRP0089P3-P049

Evaluating the Effect of Zoledronic Acid on Treatment of Primary and Secondary Pediatric Osteoporosis at Children's Hospital 1 in Vietnam
Direct

Abstract PDF
HRP0089P3-P050

Hypocalcemia Secondary to Maternal Vitamin D Deficiency
Direct

Abstract PDF
HRP0089P3-P052

A Rare Case of Familial Hypocalcemia
Direct

Abstract PDF
HRP0089P3-P053

HDR Syndrome: A Case Report of Hypoparathyroidism, Hearing Loss and Renal Agenesis
Direct

Abstract PDF
HRP0089P3-P054

Growth in The Coeliac Disease of The Child
Direct

Abstract PDF
HRP0089P3-P055

The British OsteoNEcrosis Study: A Multi-centre Prospective Study
Direct

Abstract PDF
HRP0089P3-P056

Response to Pamidronate Therapy and Pharmacogenetics in Patients with Osteogenesis Imperfecta
Direct

Abstract PDF
HRP0089P3-P057

Results of 22 Weeks of Burosumab Therapy in a Patient with Severe Bone Deformities due to XLH
Direct

Abstract PDF
HRP0089P3-P058

Severe Neonatal Hypercalcemia: A Challenging Case
Direct

Abstract PDF
HRP0089P3-P059

Assessment of Vitamin D Status in Healthy Pre-pubertal Egyptian Children
Direct

Abstract PDF
HRP0089P3-P060

Are Caucasian Children at Risk of Sub-optimal Vitamin D Levels?
Direct

Abstract PDF
HRP0089P3-P061

Incidence Rate of Vitamin D Deficiency in 12-year Old Children in Japan
Direct

Abstract PDF
HRP0089P3-P062

Idiopathic Juvenile Osteoporosis: Common Symptoms in an Uncommon Condition
Direct

Abstract PDF
HRP0089P3-P064

Hypercalcemia Associated with Increased Parathyroid Hormone-related Protein (PTHrP) in a Patient with Medulloblastoma Successfully Treated with Pamidronate
Direct

Abstract PDF
HRP0089P3-P066

A Case of Turner Syndrome with Graves' Disease and Primary Hyperparathyroidism
Direct

Abstract PDF
HRP0089P3-P067

Neonatal Hypocalcemia Revealing a Malignant Osteopetrosis
Direct

Abstract PDF
HRP0089P3-P068

Frontal Behavior Dysfunctions Revealing a Dramatic Progression of Complex Cranial Base Abnormalities in a Severe Osteogenesis Imperfecta
Direct

Abstract PDF
HRP0089P3-P069

Ionized Calcium and 25-Hydroxyvitamin D3 in Children with Steroid-sensitive Nephrotic Syndrome
Direct

Abstract PDF
HRP0089P3-P070

Hypercalcemia due to Six Newly Identified Inactivating Mutations in the CaSR Gene
Direct

Abstract PDF
HRP0089P1-P040

Poor Metabolic Control in Children and Adolescents with Type 1 Diabetes and Psychiatric Comorbidity
Direct

Abstract PDF
HRP0089P1-P041

Concealment of Type 1 Diabetes in Adolescence Affects Adherence to Treatment, Metabolic Control, and Quality of Life
Direct

Abstract PDF
HRP0089P1-P042

Risky Behaviors of Adolescents with Type 1 Diabetes in Comparison with their Healthy Peers
Direct

Abstract PDF
HRP0089P1-P043

The Effect of Social Burden on Paediatric Diabetes Outcomes
Direct

Abstract PDF
HRP0089P1-P044

Parental Anxiety about Hypoglycemia of Children and Adolescents with Type 1 Diabetes Mellitus (T1DM) and the Associated Factors
Direct

Abstract PDF
HRP0089P1-P045

Management of Diabetes During Ramadan Fasting in Children and Adolescents: Survey of Physicians' Perceptions and Practices in the Arab Society of Paediatric Endocrinology and Diabetes (ASPED) Countries
Direct

Abstract PDF
HRP0089P1-P046

Phenotypes of Diabetes and Determinants of Glycemic Control and Diabetes Complications in Haitian Youth Living in Haiti
Direct

Abstract PDF
HRP0089P1-P047

Smoke Exposure and Cardio-metabolic Profile in Youth with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P1-P048

Menstrual Cycle Disorders in Young Women with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0089P1-P049

Life Changing Decisions due to Etiological Genetic Diagnosis in Families of Children with Maturity Onset Diabetes of the Young (MODY)
Direct

Abstract PDF
HRP0089P1-P050

NBAS Gene Mutation Causes Insulin-Dependent Diabetes Mellitus in a Patient with a Multisystem Disorder Consisting Immunodeficiency and Extremely Short Stature
Direct

Abstract PDF
HRP0089P1-P051

Identification of Six Novel Mutations in Monogenic Diabetes and Congenital Hyperinsulinism and Detected by Targeted-Exome Sequencing in Korea
Direct

Abstract PDF
HRP0089P1-P052

Genetic Susceptibility to Type 1 Diabetes in Children: Analysis of Polymorphisms rs1990760 - IFIH1, rs20541 - IL13, rs231775 - CTLA 4
Direct

Abstract PDF
HRP0089P1-P053

Neonatal Diabetes as a First Symptom of IPEX Syndrom
Direct

Abstract PDF
HRP0089P1-P054

CpG Methylation Status Changes within the Protein Tyrosine Phosphatase Non-Receptor Type 22 Gene Promoters in Children and Adolescents of Greek Origin with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P1-P055

Wolfram Syndrome Case with Hypergonadotropic Hypogonadism: A Novel Mutation
Direct

Abstract PDF
HRP0089P1-P056

Different Clinical Findings in Maturity Onset Diabetes of the Young due to B-Lymphocyte Kinase Gene Mutations
Direct

Abstract PDF
HRP0089P1-P057

Three New Gene Variants (PTPRD, SYT9, and WFS1) Related to Korean MODY Children Decrease Insulin Secretion in Human Pancreatic Beta Cells
Direct

Abstract PDF
HRP0089P1-P058

Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology
Direct

Abstract PDF
HRP0089P1-P059

Impact of Diabetes During Pregnancy in Women Affected with GCK-MODY on Neonatal Health Outcome
Direct

Abstract PDF
HRP0089P1-P061

The Prevalence of Autonomic and Peripheral Neuropathy in Children and Adolescents with Type 1 Diabetic Mellitus (T1D) and Its Association with the Homozygous Status of Z-2/Z-2 Polymorphism of the Aldose Reductase Gene (AKR1B1) in the Polyol Pathway
Direct

Abstract PDF
HRP0089P1-P063

Glucose Intolerance in Survivors of Childhood Hematologic Disorders
Direct

Abstract PDF
HRP0089P1-P065

Evaluation of Diabetes Related Complications and Endothelial Dysfunction in Adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P1-P066

Complexities in the Management of New-Onset Diabetes after Transplantation (Nodat) in an Adolescent with Senior-Loken Syndrome
Direct

Abstract PDF
HRP0089P1-P067

Insulin Resistance Parameters in Children Who Were Born Very Preterm and Adequate for Gestational Age
Direct

Abstract PDF
HRP0089P1-P068

Impact on Final Height of Functional Insulin-Therapy in Type 1 Diabetes Mellitus Pediatric Patients - Experience from a Portuguese Pediatric Endocrinology Unit
Direct

Abstract PDF
HRP0089P1-P069

Triglyceride Glucose Index as a Predictor of Impaired Glucose Tolerance in Overweight and Obese Adolescents
Direct

Abstract PDF
HRP0089P1-P070

Birth Weight in Offsprings of Mothers with Gestational Diabetes Mellitus due to Mutations in GCK Gene
Direct

Abstract PDF
HRP0089P1-P071

Review and Audit of Diabetes Control in Children and Young People with Diabetes Using the FreestyleLibre Flash Glucose Scanning System (FGS)
Direct

Abstract PDF
HRP0089P1-P072

Increasing Use of Continuous Glucose Monitoring (CGM) Among Youth with Type 1 Diabetes (T1D): Icomparison of Youth from the T1D Exchange (T1DX) and the DPV Initiative
Direct

Abstract PDF
HRP0089P1-P073

Efficacy of Real-time Continuous Glucose Monitoring in Type 1 Diabetic Pre-school and School Children Treated with Multiple Daily Injections
Direct

Abstract PDF
HRP0089P1-P074

Catheter Site Selection and Anthropometric Measurements at Subjects with Type 1 Diabetes and Continuous Subcutaneous Insulin Infusion
Direct

Abstract PDF
HRP0089P1-P075

Open Source Artificial Pancreas Systems Used from Bulgarian Children and Young People with Diabetes
Direct

Abstract PDF
HRP0089P1-P076

National Survey of Usage of Continuous Glucose Monitoring in Children and Adolescents at Non Reimbursed Setting
Direct

Abstract PDF
HRP0089P1-P077

Additional Insulin is Necessary to Prevent Rise in Blood Glucose after Fat-protein-rich Meals in Type 1 Diabetes
Direct

Abstract PDF
HRP0089P1-P079

A Novel SLCA16A1 Mutation in an Infant with Hypoglycemia and Severe Metabolic Ketoacidosis
Direct

Abstract PDF
HRP0089P1-P080

Successful Transition to Sulfonylurea Therapy in Infant with Neonatal Diabetes, Developmental Delay, Epilepsy (DEND Syndrome) due to F132L ABCC8 Mutation
Direct

Abstract PDF
HRP0089P1-P082

The Comparison of the Occurrence of Beta Cells Autoantibody and Regulatory T Cells (CD4+CD25+FoxP3+) in Patients with Type 1 Diabetes Mellitus, their Siblings and Healthy Children
Direct

Abstract PDF
HRP0089P1-P083

HERV-W-Env Protein Expression in Pediatric Type 1 Diabetes Patients
Direct

Abstract PDF
HRP0089P1-P084

The Comparison of the Occurrence of Beta Cells Autoantibody and Natural Killer Cells in Patients with Type 1 Diabetes Mellitus, Their Siblings and Healthy Children
Direct

Abstract PDF
HRP0089P1-P085

T- and B-Lymphocytes Levels in Children with Type 1 Diabetes in Association with Candida Infection
Direct

Abstract PDF
HRP0089P1-P086

Coincidence of Newly Diagnosed Type 1 Diabetes Mellitus with Enteroviruses and Respiratory Tract Viruses
Direct

Abstract PDF
HRP0089P1-P087

Investigation into [beta]-cell Adaptation During Puberty
Direct

Abstract PDF
HRP0089P1-P088

The Shape of the Glucose Curve and Time to Glucose Peak During an Oral Glucose Tolerance Test as Indicators of Beta Cell Function in Obese Adolescents
Direct

Abstract PDF
HRP0089P1-P089

Features of T2DM in Adolescents with Low Titer of ICA and IAA
Direct

Abstract PDF
HRP0089P1-P090

Increasing Trend of Fasting Plasma Glucose Levels and Impaired Fasting Glucose in Non-Diabetic Korean Youth and Young Adults: A Nationally Representative Population-Based Study
Direct

Abstract PDF
HRP0089P1-P091

Screening for T2D in High Risk Egyptian Children and Adolescents Using Strip HbA1c and OGTT
Direct

Abstract PDF
HRP0089P1-P092

Association of the Sizes and Composition of HDL with Hepatic Steatosis in Adolescents with Type 2 Diabetes (T2D)
Direct

Abstract PDF
HRP0089P2-P060

Incidence of Childhood Type 1 and Type 2 Diabetes Mellitus in Qatar between 2012-2016
Direct

Abstract PDF
HRP0089P2-P061

The Prevalence of Double Diabetes in Children and Adolescents in Qatar
Direct

Abstract PDF
HRP0089P2-P062

Prevalence of Diabetes Type 1 and Type 2 in Children and Adults in Kazakhstan in 2016
Direct

Abstract PDF
HRP0089P2-P063

Detection of the Pathogenic Genes in the Diagnosis and Treatment of Hyperglycemia Infants and Children
Direct

Abstract PDF
HRP0089P2-P064

Early Diagnosis of Diabetes Type 2 in Children with Progeria Syndromes
Direct

Abstract PDF
HRP0089P2-P065

Transient Neonatal Diabetes Mellitus due to not Described Mutation in ABCC8 Gene with Different Behaviour in Affected Family Members
Direct

Abstract PDF
HRP0089P2-P066

Prothrombin Gene 20210A Mutation Heterozygosity and MTHFR Gene C677T Mutation Homozygosity Detected in a Male Toddler Experiencing Femoral Venous Thrombosis During Diabetic Ketoacidosis
Direct

Abstract PDF
HRP0089P2-P067

Frequency of Occurrence of MODY in the Population of Diabetic Patients in St. Petersburg
Direct

Abstract PDF
HRP0089P2-P069

Features of Japanese Patients with Early-Onset, Mody-Like Diabetes without Mutations in the Major Mody Genes
Direct

Abstract PDF
HRP0089P2-P070

Frequency and Etiologic Spectrum of Monogenic Diabetes in Pediatric Diabetes in a Single Academic Center
Direct

Abstract PDF
HRP0089P2-P071

Clinical Details, Molecular Genetic Analysisand Clinical Pheonotype Correlation of 14 Patients with Neonatal Diabetes from The South India - A Single Centre Experience
Direct

Abstract PDF
HRP0089P2-P072

Syndromic Patients with Negative Islet Autoantibodies should be Tested for Mongenic Diabetes: Lessons from Patient with Trmt10a Mutation
Direct

Abstract PDF
HRP0089P2-P073

A Novel Mutation in Phka2: Idiopathic Ketotic Hypoglycaemia May Represent Mild Gsdixa
Direct

Abstract PDF
HRP0089P2-P074

The Application of Next Generation Sequencing Mody Gene Panel in Greek Patients
Direct

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HRP0089P2-P075

Type 5 Monogenic Diabetes: Reportof 7 Cases
Direct

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HRP0089P2-P076

Novel Gata6-Mutation in a Boy with Neonatal Diabetes and Diaphragmatic Hernia
Direct

Abstract PDF
HRP0089P2-P077

Clinical and Genetic Characterizations of Maturity Onset Diabetes of the Young: Single Center Results
Direct

Abstract PDF
HRP0089P2-P078

Protein and Fat Effects on Post - Prandial Glucose Responses among Egyptian Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0089P2-P079

Amino Acids Plasma Profile in Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P2-P080

Betatrophin as a New Biomarker of Type 1 Diabetes Mellitus in Paediatrics
Direct

Abstract PDF
HRP0089P2-P081

Vitamin D Status among Children and Adolescent with T1DM
Direct

Abstract PDF
HRP0089P2-P082

IGF-1 Relationship with Growth Velocity in Precocious Puberty with GnRHa Treatment
Direct

Abstract PDF
HRP0089P2-P083

Relation between Hypomagnesemia and Increased Level of HbA1c in Patients with Diabetes Mellitus
Direct

Abstract PDF
HRP0089P2-P084

PID1 Alters Antilipolytic Action of Insulin and Increases Lipolysis via Inhibited the Activation of AKT/PKA Pathway
Direct

Abstract PDF
HRP0089P2-P085

The Efficacy of Tri-ponderal Mass Index and Body Mass Index in Estimating Insulin Resistance, Hyperlipidemia and Impaired Liver Enzymes During Childhood and Adolescents
Direct

Abstract PDF
HRP0089P2-P087

Translating the A1C Assay into Estimated Average Glucose Values in Children with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0089P2-P088

Relationship Between Residual Endogenous Insulin Secretion and Glycemic Control in Japanese Children and Adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P2-P089

A Curious Case of Persistent Lactic Acidosis in a Child with Diabetic Ketoacidosis
Direct

Abstract PDF
HRP0089P2-P090

An Unusual Case of an Exclusively Vegan Child with Diabetic Acidosis
Direct

Abstract PDF
HRP0089P2-P092

Hypertriglyceridemia in Type 1 Diabetes Children During Diabetic Ketoacidosis; Relation to DKA Severity and Glycemic Control
Direct

Abstract PDF
HRP0089P2-P093

Acute Mononeuropathy in an 8-Year-Old-Girl with Newly Diagnosed Type 1 Diabetes
Direct

Abstract PDF
HRP0089P2-P094

HLA-G Gene Promoter Methylation Status in Children and Adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P2-P095

Impaired Adrenal Function in Pediatric Patients with Diabetes Mellitus Type 1 Evaluated with Low-Dose Synacthen Test
Direct

Abstract PDF
HRP0089P2-P096

The Incorporation of Available Technologies for Diabetes Care Among Different Worldwide Centers: The ESPE/ISPAD Working Group on Diabetes Technology Survey
Direct

Abstract PDF
HRP0089P2-P097

Higher Percentage of Insulin Pump Users at Isle of Man (IOM) - Two Years Observational Data
Direct

Abstract PDF
HRP0089P2-P098

Use of Continuous Glucose Monitoring Systems in the Early Detection And Management of Cystic Fibrosis Related Diabetes in Children
Direct

Abstract PDF
HRP0089P2-P099

Metabolic Improvement Offered by Medtronic Minimed 640 G Associated to Transient Insulin Perfusion Suspension before Hypoglycemia in Young Patients with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P2-P100

The Glycemic Variability in Children with Diabetes Mellitus
Direct

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HRP0089P2-P101

The Levels of Blood Glucose and Counting of Carbohydrate-Fat-Protein in Diabetic Children Using Pump with Aspart and Glulisine
Direct

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HRP0089P2-P102

A Novel Missense Variant, p.(Thr405Arg), in the SLC19A2 Gene in an Infant with Thiamine Responsive Megaloblastic Anemia Syndrome Presenting with Anemia and Diabetes but with Normal Hearing
Direct

Abstract PDF
HRP0089P2-P103

Donohue Syndrome with Hypertrophic Cardiomyopathy
Direct

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HRP0089P2-P104

Age and Exocrine Pancreatic Enzyme Requirements are Major Determinants for Carbohydrate Metabolism Impairment in Children Affected with Cystic Fibrosis
Direct

Abstract PDF
HRP0089P2-P105

Post-Prandial Hyperinsulinaemic Hypoglycaemia after Oesophageal Surgery in Children
Direct

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HRP0089P2-P106

Congenital Hyperinsulinism: Clinical and Molecular Characteristics - Fluorine-18-L-Dihydroxyphenylalanine Positron Emission Tomography (F-DOPA PET) Scan Results - Treatment Responses and Short Term Outcomes of 5 Patients
Direct

Abstract PDF
HRP0089P2-P107

Congenital Hyperinsulinism in a Child with Alagille Syndrome
Direct

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HRP0089P2-P108

Severe Stress-Induced Subcutaneous and Intravenous Insulin Resistance in an Eight Year Old Boy with T1DM, Necessitating Seven Months of IV Insulin, Reversed after Psychiatric Treatment
Direct

Abstract PDF
HRP0089P2-P109

A Case of Neonatal Diabetes Due to Pancreatic Hypoplasia
Direct

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HRP0089P2-P112

A Rare Case of Diabetes Mellitus Type 1 in a Child with Neurofibromatosis Type 1
Direct

Abstract PDF
HRP0089P2-P114

Gender Characteristics of Responsibility for Their Own Health of Adolescents with Type I Diabetes Mellitus
Direct

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HRP0089P2-P116

Effect of a Reduced Fluid Replacement Regimen on the Resolution of Diabetic Ketoacidosis (DKA) in Children
Direct

Abstract PDF
HRP0089P2-P117

Prevalence of and Risk Factors for Nonadherence to Insulin Among Paediatric Type 1 Diabetes Patients in Singapore
Direct

Abstract PDF
HRP0089P2-P118

[ldquo]What do You Know About Your Diabetes?': A Qualitative and Quantitative Study of Teenagers and Young Adults' Understanding of their Disease
Direct

Abstract PDF
HRP0089P2-P119

Parental Knowledge and Attitudes Toward Diabetes Mellitus Type 1: A Cross Sectional Study
Direct

Abstract PDF
HRP0089P2-P122

A Young Type 1 Diabetic with Acute Hemichorea: Rare Central Nervous System Complications
Direct

Abstract PDF
HRP0089P3-P073

Effects of Diabetes Mellitus Type-1 on Vitamin D Status Among Children
Direct

Abstract PDF
HRP0089P3-P074

Association between Prior Toxic Stressors and Development of T2DM in Adolescents
Direct

Abstract PDF
HRP0089P3-P075

First Four Cases of Neonatal Diabetes from Kazakhstan, Almaty with Proven Mutations in KCNJ11 and INS Genes
Direct

Abstract PDF
HRP0089P3-P076

First 2 Cases of Monogenic Diabetes (MODY) from Kazakhstan, Almaty with Proven Heterozygous Mutation in Hepatocyte Nuclear Factor 1-Alpha (HNF1A) Gene
Direct

Abstract PDF
HRP0089P3-P080

Clinical and Biochemical Characteristics of Familial Type 1 Diabetes Mellitus (FT1DM) Compared to Non-Familial Type 1 DM (T1DM)
Direct

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HRP0089P3-P082

Clinical Presentation and Autoimmune Markers in Children and Adolescents with Familial Type 1 Diabetes Mellitus (FT1DM) and Familial Type 2 Diabetes Mellitus (FT2DM)
Direct

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HRP0089P3-P083

Real-world Clinical Evolution of Type 1 Diabetes Patients on Twenty Years
Direct

Abstract PDF
HRP0089P3-P084

Diabetic Capilaropathy: A Case Report
Direct

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HRP0089P3-P085

A Sibling Case of Wolfram Syndrome with Diabetes Mellitus Diagnosed within 10 Months in Early Childhood
Direct

Abstract PDF
HRP0089P3-P086

Continuous Subcutaneous Insulin Infusion in Children and Adolescents: Analysis of Initial and Follow Up Basal Rates
Direct

Abstract PDF
HRP0089P3-P087

Prevalance of Fatty Liver in Patients with Type 1 Diabetes Mellitus Attending Diabetes Clinic at Alexandria University Children's Hospital
Direct

Abstract PDF
HRP0089P3-P088

The Triad of Obesity, Acanthosis Nigricans and Diabetes Mellitus in a Newly Diagnosed Adolescent; Is This Type 1 Or Type 2 Diabetes Mellitus?
Direct

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HRP0089P3-P089

A Female Patient with Atypical Diabetes Features, Showing Heterozygous Mutations on G6PC2 (Glucose 6 Phosphatase, Catalytic Subunit 2): Does Explain All Clinical Manifestations or Is It Only Polymorphism?
Direct

Abstract PDF
HRP0089P3-P090

Clinical and Laboratory Features at the Onset of Childhood Type 1 Diabetes Mellitus in the Nortwest Region (Trakya) of Turkey
Direct

Abstract PDF
HRP0089P3-P091

Clinical and Epidemiological Features of Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0089P3-P092

Predictors of Optimal Glycemic Control in Children with Diabetes Mellitus Type 1 Receiving Pump Insulin Therapy
Direct

Abstract PDF
HRP0089P3-P093

Symptomatic Cerebral Infarction: A Rare Complication of Diabetic Ketoacidosis
Direct

Abstract PDF
HRP0089P3-P094

Our Clinical Experiences in Type 2 Diabetes
Direct

Abstract PDF
HRP0089P3-P095

The Relationship between Serum Levels of C-Peptide and the Age, BMI, and Insulin Doses in Reply to: Newly Diagnosed Type 1 Diabetic Children
Direct

Abstract PDF
HRP0089P3-P096

Serum Trace Element Levels in Children Presenting with Diabetic Ketozis and Diabetic Ketoacidosis: A Longitudinal Controlled Study
Direct

Abstract PDF
HRP0089P3-P097

Evaluation of Relation between Diabetic Education Levels of Type 1 DM Child/Adolescent and Parents and Metabolic Control
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HRP0089P3-P098

A Case of Childhood Type 1 Diabetes Mellitus Who Developed Granuloma Annulare
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Abstract PDF
HRP0089P3-P099

Case Report: De Novo Mutation of Foxp3 Causing Mild Phenotype of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Link Syndrome
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Abstract PDF
HRP0089P3-P100

Is There a Relationship between Immune-Mediated Type 1 Diabetes Mellitus and Congenital Rubella Infection?
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Abstract PDF
HRP0089P3-P101

Changes in Glycemic Control after Switching from NPH & RI to Insulin Glargine and Lispro in Children with Type 1 Diabetes Mellitus (T1DM)
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Abstract PDF
HRP0089P3-P102

When Type Mody Ii Diabetes Simulates Type I Diabetes
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HRP0089P3-P103

Epidemiological Study and Analysis of Type 1 Diabetes Comparing Patients with and Without Ketoacidosis in the Last 5 Years
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HRP0089P3-P105

Monogenic Diabetes Cause by Mutation of the Gene HNF-1A
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Abstract PDF
HRP0089P3-P106

Reversibility of Early Acute Diabetic Neuropathy (DN) in Adolescents with Type 1 Diabetes Mellitus (T1D)
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HRP0089P3-P108

Psychosocial Risks, Comorbidities and Health Events During the Follow-up of Children and Adolescents with Type 1 Diabetes
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Abstract PDF
HRP0089P3-P110

Diabetes Mellitus, Autoimmune Hemolytic Anemia, Hepatosplenomegaly and Lymphadenopathy: A Rare Association in Chinese Children
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HRP0089P3-P111

Type 1 Diabetes and Central Precocious Puberty a Rare Association
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HRP0089P3-P112

Diabetic Ketoacidosis among Egyptian Children with Type 1 Diabetes: 3-Years Study
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HRP0089P3-P113

Fructosamine Level in Type 1 Diabetes Mellitus Children Performing Ramadhan Fasting
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HRP0089P3-P114

Metformin Therapy Ina Lean Adolescent Girl with Prediabetes Dysglycemia Treated: Good Response
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HRP0089P3-P115

Association between Thyroid Stimulating Hormone and Hemoglobine A1c in Type 1 Diabetes Mellitus Children
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HRP0089P3-P116

Monogenic Diabetes in 2 Years and 4 Months Old Girl: Is it DEND?
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HRP0089P3-P117

Compliance for Monitoring of Glycemic Control in Children with Type 1 Diabetes
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HRP0089P3-P118

Ketogenic Diet in a Child with Diabetes and Global Developmental Delay
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Abstract PDF
HRP0089P3-P120

Oral Gliclazide (A Sulfonylurea) Monotherapy is Effective and Safe in the Management of T2DM in Children: A Case Report
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HRP0089P3-P121

Pediatric Stroke as the Presenting Symptom of New Onset Diabetes without DKA
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HRP0089P3-P122

Challenges in Educating New Onset Type 1 Diabetes Mellitus Patients: Can the Use of a Tablet be the Answer?
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HRP0089P3-P123

AID-GM System (Advanced Intelligent Distant - Glucose Monitoring) to Monitor Health Status and Metabolic Control of Young People with Type 1 Diabetes
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HRP0089P3-P124

Continuous Glucose Monitoring Results of Our Cases with MODY Type 2 Diabetes
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Abstract PDF
HRP0089P3-P403

Epidemiology, Demographic Criteria and Risk Factors in Type 1 DM Egyptian Children; A Single Center Study
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HRP0089P3-P407

Degludec Versus Glargine in Pediatric and Adolescent Patients with Type 1 Diabetes
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HRP0089P3-P417

Study of Children with Type 1 Diabetes Mellitus of Long Duration Attending Alexandria University Children'S Hospital
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HRP0089P3-P419

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HRP0089P1-P093

Functional Characterization of Novel and Known Genetic Variants in the Leptin Receptor (LEPR) Gene of Two Patients with Morbid Obesity
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HRP0089P1-P094

Association of Single Nucleotide Polymorphisms in TNFA, PNPLA3, ADIPOQ and APOC3 Genes with Obesity and Non-Alcoholic Fatty Liver Disease in North Indian Adolescents
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Abstract PDF
HRP0089P1-P095

Variation of Circulating Brain-Derived Neurotrophic Factor According to Gender, Body Mass Index and Metabolic Syndrome Parameters in Adolescents
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HRP0089P1-P096

Kisspeptin and the Genetic Obesidome
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Abstract PDF
HRP0089P1-P097

Circulating Exosomal miRNAs Involved in the Pathogenesis of Children Nonalcoholic Steatohepatitis
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HRP0089P1-P098

Placental Fatty Acid Profile, DNA Methylation and Adverse Metabolic Outcomes in the Offspring at School Age
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HRP0089P1-P099

Association of Serum Fibroblast Growth Factor 21 and Irisin with Insulin Sensitivity Markers and Serum Lipids in 12-year-old Children
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Abstract PDF
HRP0089P1-P100

Serum Catestatin Levels in Obese Children and Adolescents
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HRP0089P1-P101

Circulating Mots-C Levels are Decreased in Obese Male Children and Adolescents and Associated with Insulin Resistance
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HRP0089P1-P102

Plasma Adropin Levels are Associated with Lipid Characteristics Amongst Children with Obesity
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HRP0089P1-P105

Effect of a Melanocortin-4 Receptor (MC4R) Agonist, Setmelanotide, on Obesity and Hyperphagia in Individuals Affected by Alstrom Syndrome
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HRP0089P1-P106

Towards a Greater Understanding of the Pathophysiology of Obesity: Hypothalamic Obesity as a Model of Dysregulation of Appetite and Metabolic Homeostasis
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HRP0089P1-P107

Serum Uric Acid Level and Its Association with Metabolic Syndrome in Korean Adolescents
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HRP0089P1-P108

More than A Gut Feeling: Preliminary Evidence Supporting a Role for Lifestyle Habits in Shaping the Intestinal Microbiota in Childhood and Adolescence
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HRP0089P1-P109

Efficiency of Alpha-lipoic Acid in Metabolic Syndrometreatment in Children
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Abstract PDF
HRP0089P1-P110

Lipid Accumulation Product is a Predictor of Non-alcoholic Fatty Liver Disease in Childhood Obesity
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HRP0089P1-P111

Selected Serum Adipokines in Children with Irritable Bowel Syndrome
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HRP0089P1-P112

Role of Urinary NGAL and KIM-1 as Early Kidney Injury Biomarkers in Obese Prepubertal Children
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HRP0089P1-P113

Maternal Resveratrol Intake During Pregnancy and Lactation Modulates the Long-term Metabolic Effects of Maternal Nutrition on Offspring Depending on the Sex and Diet
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HRP0089P1-P114

Intrauterine Metformin Exposure and Offspring Metabolic Health at 8-Years Follow-up
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HRP0089P1-P115

Greater Maternal BMI Early in Pregnancy and Excessive Gestational Weight Gain are Independently Associated with Adverse Health Outcomes in the Offspring at Age 7 Years
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HRP0089P1-P116

Rapid BMI Gain During Later Infant Accelerates Skeletal Maturation at Prepubertal Obese Children
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HRP0089P1-P117

The More Obese - The Less Pubertal Height Gain
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HRP0089P1-P118

Longitudinal Changes in Abdominal Fat Distribution in the First Two Years of Life
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HRP0089P1-P119

Telemedicine Therapy for Overweight Adolescents: First Results of a Novel Smartphone App Intervention Using a Behavioural Health Platform
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HRP0089P1-P120

Cardiorespiratory Fitness Effectiveness is Related to Abdominal Adiposity and Insulin Sensitivity in Overweight Adolescents
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HRP0089P1-P121

Promoting Healthy Lifestyles in Youth: Preliminary from the CIRCUIT Program
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HRP0089P1-P122

Determinants of Attrition from a Healthy Lifestyle Intervention: Experience from the CIRCUIT Program
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HRP0089P1-P126

Effect of Hormonal Changes on Exocrine Pancreatic Function in Girls with Anorexia Nervosa
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HRP0089P1-P127

PCSK9 and Lp(a) Levels of Children Born after Assisted Reproduction Technologies
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HRP0089P1-P128

Rate of Accumulation of Abdominal Fat is Associated with Fasting Glucose Levels in Early Childhood
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HRP0089P1-P129

Early Menarche is Associated with Insulin Resistance and Non-Alcoholic Fatty Liver Disease in Obese Adolescents
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HRP0089P1-P130

The Frequency of Obstructive Sleep Apnea in Children with Hypothalamic and Exogenous Obesity
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HRP0089P1-P131

The Importance of Universal Lipid Profile Screening in Two to Ten Years Old Lebanese Children
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HRP0089P1-P132

Non-Invasive Measurements of Central Blood Pressure with Arterial Stiffness Indicators as a New Research Tool for Predicting Cardiovascular Risk in Children with Type 1 Diabetes Mellitus and Obesity
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HRP0089P1-P133

Severe Obesity and Cardiometabolic Comorbidities in Adolescents: Chronology of an Epidemic
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HRP0089P1-P134

Evaluation of Intraocular Pressure and Retinal Nerve Fiber Layer, Retinal Ganglion Cell, Central Macular Thickness and Choroidal Thickness Using Optical Coherence Tomography in Obese Children and Healthy Controls
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HRP0089P2-P123

Allopurinol Ameliorates Non-Alcoholic Fatty Liver Disease in Rats
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HRP0089P2-P124

Relationships of Dietary Intake and Sugar Rich Products Consumption with Hepatic Fat Content and Insulin Resistance among Children with Overweight/Obesity: The PREDIKID Study
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HRP0089P2-P125

Angiotensin-Converting Enzyme Insertion/Deletion Gene Polymorphism in Egyptian Obese Children and Adolescents: Relation to Hypertension Risk
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HRP0089P2-P126

Serum Calprotectin Level in Children: Marker of Obesity and Its Metabolic Complications
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HRP0089P2-P127

Pediatric Continuous Metabolic Syndrome Score (PsiMS score): Use in Everyday Clinical Practice
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HRP0089P2-P128

Leptin and Cytokines are Not the Best Markers for Metabolic S
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HRP0089P2-P129

Early-Life Risk Factors and Their Association with Hypertension in Spanish Children and Adolescents
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HRP0089P2-P130

A Rare Case of Diabetes Mellitus in an Adolescent: Partial Lipodystrophy
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HRP0089P2-P131

Visfatin, RBP4 and STRA6 polymorphisms' in relation with Childhood Obesity
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HRP0089P2-P132

Characteristics of Blood Lipids in Boys with Hypoandrogenia
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HRP0089P2-P133

Tri-Ponderal Mass Index: A Good Anthropometric Index to Evaluate Adiposity in Children and Adolescents
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HRP0089P2-P134

Serum Spexin Concentrations in Adolescent Females with Metabolic Syndrome, Polycystic Ovary Syndrome and Anorexia Nervosa
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HRP0089P2-P135

A Simple Relaxation Exercise Reduces Stress in Obese Youth - A Path to a Healthy Lifestyle?
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HRP0089P2-P136

Dyslipidemia and Its Related Factors in Chinese Children and Adolescents with Turner Syndrome
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HRP0089P2-P137

Severity, Duration and Phenotype of Obesity Promote Precocious Cardiovascular Sonographic Alterations in Childhood Obesity
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HRP0089P2-P138

Physical Activity Determined by Accelerometry Before and After an Integral Treatment Program in Children with Abdominal Obesity
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HRP0089P2-P140

Sex-related Differences and Effect of Puberty on Metabolic Syndrome in Obese Children and Adolescents
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HRP0089P2-P141

Associations between Total Leptin, Bio-inactive Leptin, Soluble Leptin Receptor and Anthropometrics in Children with Severe Early-onset Obesity (SEOO) - the German-Polish Study (EOL-GPS)
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HRP0089P2-P142

Children with Obesity are Taller in Early Childhood with Subsequent Catch-down Growth Until Adolescence
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HRP0089P2-P143

The Relationship between Anthropometric Measurements and Breast Milk Ghrelin and Nesfatin-1 Levels in Infants with Small for Gestational Age
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HRP0089P2-P144

Efficacy, Safety and Tolerability of Liraglutide, GLP-1 Analogue, in Indian Adolescent Population with Obesity
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HRP0089P2-P145

The Effect of Exclusive Breastfeeding and Formula Feeding on Body Composition During the First Two Years of Life
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HRP0089P2-P146

Body Composition and Cardiovascular Function in Pre-adolescent Children of South Asian and White European Origin: Relationship to Maternal Status in Pregnancy
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HRP0089P2-P147

Relation Between Cardiac Function and Anthropometric Parameters in Overweight and Obese School Boys
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HRP0089P2-P148

Evaluation of Hydration Status of Obese Children - A Pilot Study
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HRP0089P2-P149

Galanin is Positively Correlated with Insulin Resistance and Triglyceride Levels in Obese Children
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HRP0089P2-P150

Brown Adipose Tissue in Prepubertal Children: Associations with Sex and With the Sequence of Prenatal Growth Restraint and Postnatal Catch-up
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HRP0089P2-P152

Does Late Sleeping Time Results Increased Bedtime Snack? What is the Risk of this in Childhood Obesity?
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HRP0089P2-P153

Early BMI Trajectory Classes are Linked to Distinct Body Fat Partitioning Later in Childhood
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HRP0089P2-P154

Hair Cortisol Concentrations in Overweight and Obese Children and Adolescents
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HRP0089P2-P155

Associations between Body Fat Mass and Internalizing and Externalizing Behaviors and Anxiety in Children and Adolescents
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HRP0089P2-P156

Pharmacotherapy and the Effects on LDL Levels and Growth in 2 Children with Severe Familial Hypercholesterolemia
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HRP0089P2-P157

Brown Tumors in Children on Hemodialysis
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HRP0089P2-P158

The Role of Fibroblast Growth Factor 21 and Irisin in the Pathogenesis of Obesity in Childhood and Adolescence
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HRP0089P2-P159

Serum NAMPT Levels are not Associated with Parameters of Liver Function in Children and Adolescents
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HRP0089P2-P160

Obesogenic Environment and Their Influence on Adiposity on Mexican Children and Adolescents
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HRP0089P2-P161

Metabolic Alterations and Weight Status in Children at 8 Years: A Prospective Cohort Study
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HRP0089P2-P162

Correlation of Dietary Habits with Systolic Blood Pressure in Healthy Children
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HRP0089P2-P163

Evaluation of Voiding Dysfunction in Obese Children
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HRP0089P2-P164

Comparison of Antropometric and Biochemical Parameters in Obese Children with or without Primary Headache
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HRP0089P2-P165

The Protective Effect of Exclusive Breastfeeding for overweight/Obesity in Children with High Birth Weight
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HRP0089P2-P166

Determinants and Consequences of Exaggerated Adrenarche in Simple Obesity
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HRP0089P2-P167

Metabolic Alteration in Patients Affected by PseudoHypoParathyroidismo 1a (PHP1a): A Preliminary Data
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HRP0089P2-P168

Weight Loss Outcomes in Two-Year Multidisciplinary Lifestyle Intervention Program Involving Obese Children and their Parents
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HRP0089P2-P169

Relationship between Glucose and Lipid Metabolism, Inflammatory Factors and Adipokines in Children with Obesity
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HRP0089P2-P170

Development of Resistance to Sorafenib, a Multikinase Inhibitor, in Hepatocellular Carcinoma is Mediated by SIRT
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HRP0089P2-P171

Gender and Pubertal Tendencies of Plasma leptin and Dopamine Levels Depending on TaqIA DRD2 Gene Polymorphism in the Different Pediatric Obesity Classes
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HRP0089P2-P172

Iron Metabolism Disorders in Prepubertal Obese Children with and Without NAFLD
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HRP0089P2-P173

Familial Hypercholesterolemia Due to Homozygous LDLRAP1 Mutation: Variability of Phenotype and Response to Medical Therapy
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HRP0089P2-P174

CAN Triponderal Mass Index be a New Indicator in the Predicting Cardiometabolic Risk in Obese Adolescents?
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HRP0089P2-P175

Social Networks, Social Support and Weight-Related Outcomes among Adolescents
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HRP0089P2-P176

Identification of A Novel Homozygous Mutation in BBS10 in Five Children With Bardet-Biedl Syndrome
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HRP0089P2-P177

The Effects of the Birth Weight on the Fat Distribution and Fatness Parameters of the Body
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HRP0089P2-P178

Oxidative Homeostasis Dysregulation May Promote Pathogenesis of Cardio-metabolic Complications in Childhood Obesity
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HRP0089P2-P179

Body Composition Parameters, Systemic Inflammation and Metabolic Syndrome Manifestations in Children and Adolescents
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HRP0089P2-P180

Relationships between Obesity Parameters and Urinary Concentrations of Phthalates and Phenols in Korean Girls
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HRP0089P3-P125

NKX2-2 Human Mutation Causes Neonatal Diabetes followed by Severe Infantile Obesity Associated with Paradoxical Upregulated Ghrelin Levels - Do Beta-cells Secrete Ghrelin?
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HRP0089P3-P126

Tracing the Effect of the Melanocortin-4 Receptor Pathway in Obesity: Study Design and Methodology of the TEMPO Registry
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HRP0089P3-P127

BigO: Big Data Against Childhood Obesity
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HRP0089P3-P128

Exposure to Bisphenol-A and Phtalates in Obese Girls
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HRP0089P3-P129

Obesity of Childhood and Ambulatory Glucose Monitorization
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HRP0089P3-P130

Familial Partial Lipodystrophy, Importance of Family History - A Case Report
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HRP0089P3-P131

Development of Severe Obesity in a Children with a Brainstem Tumor
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HRP0089P3-P132

Correlation Between Obesity, BMI and Insulin Resistance in Bulgarian Children
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HRP0089P3-P133

Nonclassical Manifestation of PWS
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HRP0089P3-P134

Metabolic Parameters in Children with Syndromic Obesity
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HRP0089P3-P135

Cut-off for the Follow-up of Obese Children: Cynicism or Realism?
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HRP0089P3-P136

Proximal Microdelection 16p11.2 Syndrome
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HRP0089P3-P138

A Compound Heterozygote Mutation in a Chinese Patient Affected with Methylmalonic Acidemia
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HRP0089P3-P139

Lymposomal Acid Lipase Deficit in Patients with Hypercholesterolemia
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HRP0089P3-P140

Hepatic Steatosis and its Relationship with the Metabolic Syndrome
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HRP0089P3-P141

Serum Hepcidin and Ferritin in Prepubertal Obese Children
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HRP0089P3-P142

Osse Registry for Patients with Lipodystrophy Run by the European Consortium of Lipodystrophy (ECLip)
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HRP0089P3-P143

Acanthosis Nigricans in Obese Children and Adolescents in relation to Severity of Obesity and Insulin Resistance
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HRP0089P3-P144

Serum Uric Acid and Its Correlation with Metabolic Syndrome Factors in Simple Obesity Children
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HRP0089P3-P145

Thyroid Function, Lipid Profile and Carbohydrate Metabolism Parameters in Patients with Alstrom Syndrome
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HRP0089P3-P146

Does the Level of Studies of Parents Influence the Follow-up of the Recommendations of the Nutritional Pyramid?
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HRP0089P3-P147

Bariatric Surgery as Treatment of Primary Pseudotumor cerebriin a Male Adolescent: Case Report
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HRP0089P3-P148

Investigation of Pubertal Effect on Thyroid Volume and IGF-1 Changes in Morbid Obese Children
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HRP0089P3-P149

The Effect of Vitamin D Supplementation on Metabolic Syndrome Parameters in Overweight and Obese Children and Adolescents in Greece
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HRP0089P3-P150

Mother's Obesity and High Child's Waist Circumference are Predictive Factors of Severe Child's Obesity: An Observational Study in French Guiana
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HRP0089P3-P151

Lipidogram, Leptin-and Adiponectinaemia in Teenagers and Adolescents with Metabolic Syndrome
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HRP0089P3-P152

Metabolic Endotoxemia in Egyptian Obese Children and Adolescents
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HRP0089P3-P153

Resting Metabolic Rate and the Development of Metabolic Disorders in Obese Children
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HRP0089P3-P154

Relation of Screen-Time (Phone-Computer-TV-Online Games) and Physical Activity with Childhood Obesity
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HRP0089P3-P155

Effect of Three-Month Diet and Physical Activity on Adipokines and Inflammatory Status in Children with Metabolic syndrome
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HRP0089P3-P156

Neck Circumference and Lipid Profile in Adolescents with Overweight/Obesity
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HRP0089P3-P157

A Not So 'Simple Obesity'
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HRP0089P3-P159

Compliance of Obese Children and Their Family to the Directions of a Pediatric Endocrinology Medical Office
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HRP0089P3-P160

Risk Factors and Comorbidities of Childhood Obesity
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HRP0089P3-P161

Autonomic Nervous System - Inflammation Link: A New Independent Mechanism for Homeostasis
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HRP0089P3-P162

Effects of a Brief Physician Delivered Counseling on Childhood Obesity
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HRP0089P3-P166

Assessment of Obesity in Children with Achondroplasia and Hypochondroplasia
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HRP0089P3-P167

Correlation of Lipoprotein(a) Levels and Family History of Cardiovascular Disease in a Sample of Overweight/obese Children and Adolescents
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HRP0089P3-P168

Beneficial Effect of Metformin Treatment in Obese Children and Adolescents
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HRP0089P1-P135

Cardiac and Vascular Assessments in Small- vs Appropriate-for-Gestational-Age Infants at Ages 1 and 2 Years
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HRP0089P1-P136

Bone Maturation as a Predictive Factor of Catch-up Growth During the First Year of Life in Born Small for Gestational Age Infants: A Prospective Study
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HRP0089P1-P137

Neonatal Screening Tests in Premature Newborns in Southern Brasil
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HRP0089P1-P138

Measurement of Estradiol and Testosterone in Umbilical Cord Blood by Gas Chromatography-Tandem Mass Spectrometry (GC-MS/MS); Comparisons with Radioimmunoassay (RIA)
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HRP0089P1-P139

Transient Neonatal Iatrogenic Hypothyroidism due to Iodinated Contrast
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HRP0089P1-P140

Sexual Dimorphism of IGF1 and IGF2 Expression in the Neonatal Rat Brain
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HRP0089P2-P181

Clinical characteristics of Congenital Hyperinsulinism Caused by Dominant KCNJ11/ABCC8 Mutations
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HRP0089P2-P182

Clinical Characterstics, Genotype-Phenotype Correlations and Follow Up of Patients with Congenital Hyperinsulinaemic Hypoglycaemia; Single Center Experience from a Southeastern City of Turkey
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HRP0089P2-P183

Congenital Hyperinsulinism: Management and Outcome in West of Scotland
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HRP0089P2-P184

20 Cases of Congenital Hyperinsulinism in Ukraine
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HRP0089P2-P185

Nifedipine Therapy in Hyperinsulinaemic Hypoglycaemia Due to Mutations in the PMM2 Gene Improves Fast Tolerance, Stabilises Blood Glucose Profile, and Enables Rationalisation of Treatments for Glycaemic Control and Hypertension: The First Reported Trial in 3 Patients in a Tertiary Centre
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HRP0089P2-P186

Potentially Modifiable Predictors of Adverse Neonatal Outcomes in Women with Gestational Diabetes Mellitus (GDM)
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HRP0089P2-P187

A Boy with Diazoxide Unresponsive Congenital Hyperinsulinism due to a Homozygous ABCC8 Missense Mutation Previously Reported to be Dominant
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HRP0089P2-P188

Diazoxide Unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation
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HRP0089P2-P189

Neonatal Hypoglycaemia: Unchanged Risk of Neurodevelopmental Impairment, But Sex-Specific Decreased Fine Motor Function and Increased Internalizing Behaviour at School Age
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HRP0089P2-P190

Atypical Hepatoblastoma and Wilm's Tumour in an Infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism
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HRP0089P2-P191

Association between Rubenstein-Taybi Syndrome and Hyperinsulinaemic Hypoglycaemia
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HRP0089P2-P192

Hyperinsulinemic Hypoglycemia in Congenital Disorder of Glycosylation Type-1a (CDG-1a)
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HRP0089P2-P193

A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello Syndrome
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HRP0089P2-P195

The Benefit of Universal Neonatal Screening for Hypoglycemia
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HRP0089P2-P196

Prematurity of 23 or Less Weeks' Gestation is a Risk for Transient Late-Onset Hyperglycemia in Neonates
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HRP0089P2-P197

An unusual cause of neonatal hyperglycemia - case report
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HRP0089P2-P198

Neonatal Hypocalcemia Due to Maternal Hypovitaminosis D: A Cohort of Children in a Region of Northern Spain
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HRP0089P2-P199

Evaluation of Vitamin D Status and Its Correlation with Gonadal Function in Children at Mini-puberty
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HRP0089P2-P200

Systemic Pseudohypoaldosteronism Type 1 Due to 3 Novel Mutations in SCNN1A and SCNN1B Genes; Report of 3 Cases
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HRP0089P2-P201

Postnatal Growth of Infants with Neonatal Diabetes: Insulin Pump (CSII) Versus Multiple Daily Injection (MDI) Therapy
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HRP0089P2-P202

Serum Vaspin Concentration in Full-term, Appropriate-for-Gestational-Age Newborns: Effect of Early-Onset Infections
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HRP0089P2-P203

First Three Years of The Congenital Adrenal Hyperplasia Neonatal Screening Program of the State of Parana, Southern Brazil
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HRP0089P2-P204

Assessment of the Stretched Penile Length in Sri Lankan Newborns
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HRP0089P2-P205

Auxological Catch Up Growth and Evaluation of Spontaneous Motility in the Term Newborn Small for Gestational Age Employing the Prechtl Assessment of General Movements
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HRP0089P3-P171

Comparison of Metabolic Parameters of Children's Blood Depending on the Level of Mother's Glycemia During Pregnancy
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HRP0089P3-P172

Forty patients with persistent, non-focal congenital hyperinsulinism: Urgent need for new treatment modalities
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HRP0089P3-P173

Outcome of Eight Patients with Congenital Hyperinsulinism (CHI) Studied with 18[F]Dihydroxyphenyl-Alanine Positron Emission Tomography Imaging (18F-DOPA-PET-CT) in Argentina
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HRP0089P3-P175

Neonatal Diabetes Mellitus in Vietnam National Children Hospital
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HRP0089P3-P176

Axillary Temperature Relation to Blood Serum Insulin-like Growth Factor-I in the Not-life-Threatened Newborn: Relevance of Preterm Birth
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HRP0089P3-P177

Birth Estimated Brain Weight Relation to Ratios between Insulin-like Growth Factor-II and Insulin-like Growth Factor Binding Protein-3 in the Not-life-threatened Newborn: Relevance
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HRP0089P3-P178

Congenital Hyperinsulinism in Children with Beckwith-Wiedemann Syndrome
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HRP0089P3-P179

Comparison of the Phenylketonuria Phenotypes in Qazvin Province Before and After Neonatal Screening Until 2017
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HRP0089P3-P180

From Hypoglycemia to Hyperglycemia
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HRP0089P3-P181

Population Screening of Hypophosphatasia. A Metabolopathy to Consider. National Multicentric Study
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HRP0089P3-P182

Dumping Syndrome in a Neonate with Esophagical Atresia Surgery
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HRP0089P3-P183

Diagnosis and Treatment of Persistent Hyperkalemia in Newborn Twins - Rare Case Report of Gordon Syndrome
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HRP0089P3-P184

Mutation in UCP2 Gene: A Rare Cause of Hyperinsulinemic Hypoglycaemia Syndrome in a Small-for-Gestational Age Newborn
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HRP0089P3-P185

Hyperinsulinemic Hypoglycaemia Syndrome in Small-for-Gestational Age Newborns: Clinical Characteristics and Genetic Study
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HRP0089P3-P186

Pediatric Insulinoma: A Case Report
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HRP0089P3-P188

Weight Outcome in Infants with Prolonged Hyperinsulinemic Hypoglycemia Treated with Diazoxide vs Those with Spontaneous Resolution
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HRP0089P3-P189

Neonatal Hyper- and Hypoglycaemia; Widening the Clinical Phenotype of Transient Neonatal Diabetes Mellitus due to 6q24 Methylation Defects
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HRP0089P3-P191

Transient Central Hypothyroidism due to Maternal Graves' Disease
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HRP0089P1-P141

Autosomal Dominant Growth Hormone Deficiency due to a Novel c.178G>A Mutation in the GH1 Gene Causing Instability of the Mutant GH Protein (p.Ala34Thr)
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HRP0089P1-P142

Growth Hormone Deficiency due to Whole-Gene Deletion of GHRHR
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HRP0089P1-P143

Severe Pre- and Postnatal Growth Retardation in a Child Harboring a Novel Homozygous IGF1 Gene Mutation
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HRP0089P1-P145

Response to Growth Hormone in Patients with Isolated Familial Growth Hormone Deficiency due to RNPC3 Mutations
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HRP0089P1-P146

Laron Syndrome Patients have an Abnormal Plasma Amino Acid Pattern
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HRP0089P1-P147

Serum IGFBP-2 Concentration in Neonates with Potential Diagnosis of Growth Hormone Deficiency (GHD)
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HRP0089P1-P149

Assesment of SDF-1 and Ang-1 and Ang-2 in Children with Growth Hormone Deficiency before and after 1- year Therapy with Recombinant Growth Hormone
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HRP0089P1-P150

Total Sum of Growth Hormone Values Obtained from Growth Hormone Stimulation Test May be Useful in the Diagnosis of Prepubertal Children with Idiopathic Growth Hormone Deficiency
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HRP0089P1-P152

Microalbuminuria and Glomerular Filtration Rate in SGA Born Young Adults
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HRP0089P1-P153

Testing the Performance of a Preexisting Growth Prediction Model in a Cohort of Prepubertal Patients Born Small for Gestational Age (SGA) Receiving GH Treatment in PATRO Children
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HRP0089P1-P154

Early Onset GH Replacement in GH Deficiency: Is Neonatal Hypoglycemia Important for Long Term Follow-Up?
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HRP0089P1-P155

Prevalence of Diabetes among Children Treated with Growth Hormone in Israel
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HRP0089P1-P156

The Effect of Growth Hormone Treatment in Children after Hematopoietic Stem Cell Transplantation
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HRP0089P1-P157

EasypodTM Connect Observational Study: The Italian Experience
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HRP0089P1-P158

Patients and Caregivers Perspectives on a Mobile App that Tracks Adherence and Outcomes in Children with Growth Disorders Treated with Recombinant Human Growth Hormone (r-hGH)
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HRP0089P2-P207

Clinical and Preliminary Molecular Description of a Cohort of Patients with Growth Retardation due to Severe Primary IGF1 Deficiency (GROWPATI Study)
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HRP0089P2-P208

A Novel, Synonymous, Heterozygous, Splicing Variant Affecting the Intracellular Domain of the Growth Hormone Receptor: Causality for Mild Growth Impairment and IGF-I Deficiency in an Affected Patient?
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HRP0089P2-P209

A Novel Mutation of Type I Insulin-like Growth Factor Receptor (IGF1R) Gene in a Severe Short Stature Pedigree Identified by Targeted Next-generation Sequencing (NGS)
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HRP0089P2-P210

Severe Short Stature, Growth Hormone (GH) Deficiency, Hypospadias, and Microcephaly: New Insights into the Role of Chromosome 4 Long Arm Duplication
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HRP0089P2-P211

Growth Hormone Treatment for Short Stature Associated with TRNT1 Deficiency: A Case Series
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HRP0089P2-P212

Case Report: Novel Case of Short Stature and Co-occurrence of SHOX Gene Mutation and Fanconi Anemia
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HRP0089P2-P213

Different Genetic Causes of Short Stature in a Family
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HRP0089P2-P214

Incidence of Cranial MRI Abnormalities in Patients with Isolated Growth Hormone Deficiency: 20 Years of Results
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HRP0089P2-P215

Systematic Prospective Study of Eye Funduscopy Before and After Starting Treatment with Growth Hormone in 290 Patients
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HRP0089P2-P216

Incidence and Prevalence of GH Deficiency in the Russian Federation - An Analysis of Two Registries
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HRP0089P2-P217

The BSPED National GH Audit: Trends in Prescribing from 2013-2016
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HRP0089P2-P218

The Rationale and Design of TransCon GH
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HRP0089P2-P219

Baseline Demographics of the TransCon GH Phase 3 heiGHt Trial
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HRP0089P2-P220

The ZOMATRIP Study: Four Year Combination Therapy of GH and GnRHa in Girls with a Short Predicted Adult Height During Early Puberty: Adult Height Outcome
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HRP0089P2-P221

Growth Hormone Treatment in Children Born Small for Gestational Age (SGA)
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HRP0089P2-P222

Height Perception of Children with GH Deficiency: Influencing Factors and Links to Psychosocial Functioning
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HRP0089P2-P223

Health Lifestyle and Obesity of Adult Patients with Congenital Isolated Growth Hormone Deficiency Treated in Childhood
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HRP0089P2-P224

Factors Influencing Health Related Quality of Life in Children/Adolescents with GH Deficiency
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HRP0089P2-P225

Health-Related Quality of Life and Psychosocial Functioning in Young Adults Born SGA after GH/GnRHa Treatment
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HRP0089P2-P226

Adherence to Treatment in Growth Hormone Deficient and Small for Gestational Age Patients Naive to EasypodTM in Mexico: Final Results of the EasypodTM Connect Observational Study (ECOS)
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HRP0089P2-P227

Growth Pattern and Final Height Outcome in Children with Septo-optic Dysplasia and Isolated Hypopituitarism Treated with rhGH in a Single Centre
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HRP0089P2-P228

Reliability of Clonidine Testing for the Diagnosis of Growth Hormone Deficiency in Children and Adolescents
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HRP0089P2-P229

Area under the Curve of Growth Hormone, An Additional Tool in Assessing Stimulation Test Results
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HRP0089P2-P230

Evaluation of Spontaneous Nocturnal GH Secretion: Noe Versus Two Consecutive Nights
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HRP0089P2-P231

Relationship between Growth Velocity and Change of Serum Insulin-Like Growth Factor-1 (IGF-1), Serum IGF Binding Protein-3 (IGFBP-3) Concentrations, and IGFBP-3 Promoter Polymorphism during Gonadotropin-Releasing Hormone Agonist (GnRHa) Treatment
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HRP0089P2-P232

The Predictive Role of IGF-1 on Irradiation-Dependent Growth Hormone Deficiency (GHD) in Childhood Cancer Survivors (CCS)
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HRP0089P2-P234

High Protein Nutritional Supplementation Increases Serum IGF-I Concentrations in Short Children with Low IGF-I
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HRP0089P2-P235

Hormonal Predictors of Growth Hormone Therapy Effectiveness in Children with Short Stature - Evidence from Neural Prediction Model for Final Height
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HRP0089P2-P236

Artificial Neural Networks for Prediction Final Height in Children with growth Hormone Deficiency
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HRP0089P2-P237

Predictors of Poor Response to Growth Hormone Therapy in Children with Short Stature - Evidence from Neural Prediction Model for Final Height
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HRP0089P2-P238

Growth Hormone Therapy and Its Challenges in GH Deficient Cases in a Multinational Population-a Sneak-Peek
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HRP0089P3-P192

Good Growth Response to Growth Hormone Therapy in Short Children with Normal Growth Hormone Secretion
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HRP0089P3-P194

Growth Hormone Treatment: Does Timing Matter?
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HRP0089P3-P195

Support for Patients Treated with Growth Hormone to Reach their Growth Potential: Addressing Adherence Barriers through Personalised Behavioural Patient-support Programmes
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HRP0089P3-P196

Main Discrepancies between Predicted and Observed Growth Responses with iGRO in Children Treated with GHr in Spain
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HRP0089P3-P197

Adherence and Long-term Outcomes of Therapy in Pediatric Subjects in Greece Using Easypod Electromechanical Device for Growth Hormone Treatment: The Phase IV Multicentre Easypod Connect Observational Study (ECOS)
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HRP0089P3-P198

Growth Hormone Deficiency in Neurofibromatosis: Report of Four Cases
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HRP0089P3-P199

Extremely Low Body Mass Index Negatively Impact the Response to Growth Hormone Treatment in Children with Growth Hormone Deficiency
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HRP0089P3-P200

Small for Gestational Age (SGA) Patients with Premature Treatment Discontinuation: Their Journey in French Real-life Settings
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HRP0089P3-P201

Effects on Near-adult Height and Safety of Recombinant Human Growth Hormone in Growth Hormone Deficiency and Turner Syndrome Patients: Results from the LG Growth Study
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HRP0089P3-P202

Final Adult Height After Growth Hormone Treatment in Patients with Turner Syndrome
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HRP0089P3-P203

Results of Mecasermin Treatment in Pediatric Patients Evaluated for Severe and Partial Primary Deficiency of IGF-1
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HRP0089P3-P204

Children Born Small for Gestational Age Treated with Growth Hormone: Evolutionary Aspects
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HRP0089P3-P205

Small for Gestational Age (SGA) Patients in Real Life French Clinical Practice: What is the Difference Between Good and Poor Responders to GH Treatment
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HRP0089P3-P206

Body Mass Index (BMI) in Patients with Growth Hormone Deficiency (GHD) at Diagnosis, One Year and Two Years After Treatment with Growth Hormone (GH)
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HRP0089P3-P207

Erythropoietin and Granulocyte Macrophage Colony Stimulating Factor Levels in Growth Hormone Deficient Children after 1 Year of Growth Hormone Therapy
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HRP0089P3-P208

Cost-effectiveness of Growth Hormone Therapy in Children in Russia
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HRP0089P3-P209

Vitamin D Status in Children with Isolated Idiopathic GH Deficiency (GHD) in North and Central Greece
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HRP0089P3-P210

A Pilot Study for Comparing Efficacy and Safety of the CinnaTropin® to the Reference Recombinant Human GH in Children with Isolated GH Deficiency and Multiple Pituitary Hormone Deficiency
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HRP0089P3-P211

Study of the Effectiveness of GH in Children Born Small for Gestational Age in an Area of Northwestern Spain and its Associated Factors
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HRP0089P3-P212

Height Velocity and Height Gain in the First Year of GH Treatment: Predictive Factors of Good Statural Response in Small for Gestational Age (SGA) Patients
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HRP0089P3-P213

Role of Insulin like Growth Factors on the Growth Parameters in Children with Acquired Hypothyroidism: An Analysis
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HRP0089P3-P214

Two Siblings with Short Stature
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HRP0089P3-P215

RHGH Replacement Therapy and Side-Effects: A Retrospective Study of 10 Years
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HRP0089P3-P217

Comparison the Recombinant Human GH (rhGH) Treatment in Children with Idiopathic Short Stature (ISS) and GH Deficiency (GHD)
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HRP0089P3-P218

Bone Age Maturation During the Three Years of GH Treatment in Patients with Idiopathic GH Deficiency and Idiopathic Short Stature: Analysis of Data from LG Growth Study
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HRP0089P3-P398

Recombinant Growth Hormone Therapy in Prepubertal Children with Idiopathic Short Stature in Korea: A Phase III Randomized Trial
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HRP0089P1-P159

Does X-Chromosome Gene Dosage Determine Growth and Phenotypic Features in Turner Syndrome with 45,X/46,XX Mosaicism on Standard Karyotyping? A Cross-Sectional Analysis of the French National Rare Disease Network Database
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HRP0089P1-P162

Comparing the Cumulative Dose of Growth Hormone Therapy Using Body Weight-Based Dosing Versus Body Surface Area-Based Dosing in Children with Turner Syndrome - Data from the ANSWER Study
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HRP0089P1-P163

The Association between Growth Hormone Dose and Short-Term Height Outcomes in a Large Cohort of Paediatric Patients with Turner Syndrome: Real-World Data from the NordiNet® International Outcome Study (IOS) and ANSWER Program
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HRP0089P1-P164

Changing Patterns of Growth in Prader-Willi Syndrome
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HRP0089P1-P166

Safety and Effectiveness of Growth Hormone Treatment in Patients with Prader-Willi Syndrome under 2 Years of Age in a Reference Hospital
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HRP0089P1-P167

Improved Mental and Motor Development During 3 Years of GH Treatment in Very Young Children with Prader-Willi Syndrome
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HRP0089P1-P168

GH Response to GHRH and Arginine in Previously GH-Treated Young Adults with Prader-Willi Syndrome
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HRP0089P1-P169

A Novel Type of Pubertal Height, Weight, and BMI Reference, Aligned for Onset of Puberty
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HRP0089P1-P170

Evaluating Cut-offs for Automatic Growth Screening in Swedish Children - Using the Finnish Growth Monitoring Algorithm
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HRP0089P1-P171

Prospective Study of Growth in Swedish Children Treated with Modified Ketogenic Diet
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HRP0089P1-P172

Early Gut Microbiota and childhood Growth
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HRP0089P1-P173

Clinical and Radiological Manifestations in a Large Swedish Family with a Pathogenic Heterozygous ACAN Variant
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HRP0089P1-P174

Identification of ADAMTS6 as a Novel Candidate Gene for Idiopathic Short Stature with Advanced Bone Maturation
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HRP0089P1-P175

Dual Function of the Retinoic Acid Catabolizing Enzyme CYP26C1 - Underlying Idiopathic Short Stature and Modifying Disease Severity in SHOX Deficiency
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HRP0089P1-P176

Growth Plate Disorders are the Main Cause of Severe Familiar Short Stature in Children Classified and Treated with Growth Hormone as SGA or GHD
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HRP0089P1-P177

Genetic Investigation of Children with Syndromic Prenatal Onset Short Stature
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HRP0089P1-P178

Identification of Three Novel Mutations in 10 Pediatric Patients with Unexplained Syndromic Short Stature Identified by Targeted Exome Sequencing in Korea
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HRP0089P1-P179

Beckwith Wiedemann Syndrome: First International Consensus Regarding Diagnosis and Clinical Management
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HRP0089P1-P180

Silver Russell and Beckwith-Wiedemann Syndromes: Mosaic Distribution of Epigenetic Anomalies
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HRP0089P1-P182

Year-one Effectiveness and Overall Safety of NutropinAq® for Growth Hormone Deficiency (GHD) and Other Paediatric Growth Disorders: Completion of the International Cooperative Growth Study (iNCGS) European Registry
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HRP0089P1-P184

Characteristics, Effectiveness and Safety Data for Patients with Growth Failure Treated with Recombinant IGF-I (rhIGF-I) and Achieving Adult or Near-adult Height (AH): Results from the European Increlex® Growth Forum Database (EU-IGFD) Registry
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HRP0089P1-P186

Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Six Patients
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HRP0089P1-P187

A Novel Deadly Variant in the TP53 Gene Causing Li-Fraumeni Syndrome. The Importance of Clinical Awareness and the Contribution of Molecular Diagnosis in Active Prevention Within Families with Multiple Tumor Incidents at a Young Age
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HRP0089P1-P188

Mutations in SHOX, GHR and IGFALS Genes Among Indian Children with 'Idiopathic Short Stature'
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HRP0089P2-P239

Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype
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HRP0089P2-P240

The Validation of an Automated Bone Age Assessment in Girls with Turner Syndrome - A Pilot Study
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HRP0089P2-P241

Turner Syndrome and Autoimmune Thyroid Disease: Pecularities of Evolution in 93 Turner Syndrome Patients
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HRP0089P2-P242

Unusual Clinical Manifestations in Turner Syndrome
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HRP0089P2-P243

Effect of Combined GH and Estrogen Treatment on the Lipid Profile and Systolic Function of the Left Ventricle in Girls with Turner Syndrome (TS)
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HRP0089P2-P244

Familial Turner Syndrome: Case Report
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HRP0089P2-P245

Clinical Review of Seven Patients Affected with 49,XXXXY Syndrome
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HRP0089P2-P246

Poor Weight Gain in Prader-Willi Syndrome - Not Always Over-restriction Consider Coeliac Disease
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HRP0089P2-P247

GH Unmasked Laryngomalacia and worsened Obstructive Sleep Apnea in Infants with Prader-Willi Syndrome
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HRP0089P2-P248

How Frequent Are Growth Charts Used in Paediatric Clinics? An Audit of Growth Chart Use in a District General Hospital in Scotland
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HRP0089P2-P249

GrowInform - A Campaign for Early Diagnosis and Treatment of Growth Disorders
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HRP0089P2-P250

Growth and Body Composition of Term Healthy Indian Infants from Birth to 2 Years of Age
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HRP0089P2-P251

Growth, Body Composition and Metabolic Parameters during Childhood in a Cohort of Children Born with a Small for Gestational Age
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HRP0089P2-P252

Final Results of NordiNet® International Outcome Study: Key Outcomes in Paediatric Patients
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HRP0089P2-P253

Influence of Puberty on Adult Height of SGA Children Treated with GH
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HRP0089P2-P254

Burden and Impacts of Daily Recombinant Human Growth Hormone (r-hGH) Injections in Growth Hormone Deficient (GHD) Paediatric Patients
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HRP0089P2-P255

Clinical and Cost-Effectiveness of GH Treatment for Children in Wales
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HRP0089P2-P256

Bone Mineral Density and Body Composition of Young Adults Who Were Born Small for Gestational Age and Treated with Growth Hormone, after Treatment Completion
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HRP0089P2-P258

Clinical and Molecular Analyses of 24 Patients with Beckwith-Wiedemann SYNDROME
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HRP0089P2-P259

Unusual Case of Combination of Beckwith-Wiedemann Syndrome and SHOX Gene Deficiency
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HRP0089P2-P260

An Irish Regional Study of Paediatric Growth Hormone Deficiency (CO-GHD): Classification of Causes and Factors Associated with Persistent GHD at Transition
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HRP0089P2-P261

Two Different Variants of Short Stature Homeobox-Containing Gene (SHOX) Mutation in the Same Family
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HRP0089P2-P262

Identification of a Novel Heterozygous ACAN Mutation in a Patient with Non-Syndromic Short Stature
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HRP0089P2-P263

Genetic Investigation of SHORT Stature: A Case Report of Complex Constitutive Rearrangement Involving Chromosome 15
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HRP0089P2-P264

Targeted/Exome Sequencing Identified Mutations in 55 Chinese Children Diagnosed with Noonan Syndrome and a Autosomal Recessive form Associated with LZTR1 Variants
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HRP0089P2-P265

A Novel Heterozygous Missense Variant in the LZTR1 Gene as a Cause of Noonan Syndrome
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HRP0089P2-P266

A Novel FGFR1 Mutation in Kallmann Syndrome with Growth Hormone Deficiency
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HRP0089P2-P268

A New Mutation in IHH Gene Causing Severe Short Stature
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HRP0089P2-P269

Case Report: Ellis Van Creveld Syndrome With a Novel Mutation
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HRP0089P2-P270

A Homozygous Pathogenic Variant in the TRHR Gene in a Boy Who Presented With Severe Familial Short Stature and Central Hypothyroidism
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HRP0089P2-P271

Unexpected Growth Patterns in Branchio-Oto-Renal Syndrome
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HRP0089P2-P272

Mild Autistic Spectrum Disorder in a 33 Year-old Male Japanese Patient with Temple Syndrome
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HRP0089P2-P273

Seventeen-year Observation in a Japanese Female Case of Tatton-Brown-Rahman Syndrome: An Overgrowth Syndrome with Intellectual Disability
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HRP0089P2-P274

KBG Syndrome: Our Experience and Unreported Clinical Features
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HRP0089P2-P275

Growth of Infants Born by Intracytoplasmic Sperm Injection (ICSI) Technique
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HRP0089P2-P276

Earlier Mother's Age at Menarche is a Risk Factor of Daughter's Early Menarche and Short Stature in Young Korean Female: Epidemiologic Study
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HRP0089P2-P277

Pulling the Brakes - 'Catch Down Growth': A Phenomenon for Achieving Mid-parental Height Centile After Acquired, All-cause, Brain Injury
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HRP0089P2-P278

Effects of Inhaled Corticosteroids and Montelukast on Growth and BMI in Children with Asthma
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HRP0089P2-P280

Skeletal Disproportion and Growth Impairment in Glucocorticoid Treated Boys with Duchenne Muscular Dystrophy
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HRP0089P2-P281

A Novel Mutation in the SLC2A2 Gene in a 19-Year-Old Female with Diabetes Mellitus and Renal Tubular Acidosis: A Therapeutic Conundrum
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HRP0089P2-P282

Vesico-Ureteral Reflux and Effect on Growth Indices
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HRP0089P3-P219

Is Growth Hormone Deficiency a Contributor to Short Stature in Cutis Laxa Syndrome?
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HRP0089P3-P220

Effect of Sickle Cell Disease on Growth and Puberty
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HRP0089P3-P221

Two Siblings with Alstrom Syndrome
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HRP0089P3-P222

Development of an Online Learn-pro Module to Support Health Care Professionals Knowledge about Growth and Puberty
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HRP0089P3-P223

Coeliac Disease in Turner Syndrome More Frequent Than Expected
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HRP0089P3-P224

A 14-Year-Old Boy with Simpson-Golabi-Behmel Syndrome - Case Report
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HRP0089P3-P225

Central Precocious Puberty in a Girl with Silver Russell Syndrome
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HRP0089P3-P226

Etiologies of Short Stature in Pedaitric Endocrine Clinic in Northwest Region (Trakya) of Turkey
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HRP0089P3-P227

Auditing Presentation, Investigations and Management of Turner's Syndrome
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HRP0089P3-P228

Children Born Small for Gestational Age: Catch-up Growth During the First Four Years of Life
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HRP0089P3-P229

A Novel Heterozygous Pathogenic Variant in PORCN Gene Causing Focal Dermal Hypoplasia with Short Stature: Case Report and Literature Review
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HRP0089P3-P230

Endocrinological Evaluation of Girls with Turner Syndrome Attending Alexandria University Children's Hospital
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HRP0089P3-P231

A Long Follow-up in a Young Patient with Atypical Progeroid Syndrome
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HRP0089P3-P232

GH Treatment in Kabuki Syndrome: A Case Report
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HRP0089P3-P233

GH Treatment in Oto-Spondylo-Megaepiphyseal Dysplasia: A Case Report
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HRP0089P3-P234

Hepatic Glycogen Synthasedeficiency Associated with Growth Hormone Deficiency: A Case Report
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HRP0089P3-P235

Analysis of Genetic Mutations in a Chinese Patient Affected with Noonan Syndrome
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HRP0089P3-P236

A Novel Homozygous Mutation in ERCC8 Cause Cockayne Syndrome a in a Chinese Family
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HRP0089P3-P237

Growth Hormon Deficiency in Identical Twins with Gitelman Syndrome due to Compound Heterozygous Mutation (p.R80fs*35/p.K957X) of the SLC12A3 Gene and the Evaluation of the Response to Growth Hormone Replacement Therapy
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HRP0089P3-P238

Hypothyroidism and Growth Hormone (GH) Deficiency, a Spotlight on De Novo Chromosomal 20p11.2 Deletion
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HRP0089P3-P239

Pharmacoeconomic and Adherence Analysis in Growth Hormone According to Galenic Presentation: In Vivo Study vs In Vitro
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HRP0089P3-P240

The Expression of Cytokines in SGA Children Throughout Lactation Allows to Characterize Early the Type of Cath-up
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HRP0089P3-P241

Small Stature: A Singular Difference for Accessing to Job
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HRP0089P3-P242

A Case of Hutchinson-Gilford Progeria Syndrome (HGPS) due to a Pathogenic LMNA Variant c.433G>A (p.Glu145Lys): Growth Hormone Administration Failed to Improve Growth and Long-term Outcome
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HRP0089P3-P243

Increased Serum Activity of Liver Aminotransferases in Young Patients with Turner Syndrome
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Abstract PDF
HRP0089P3-P246

Microduplication of 3p25.3 and 4p23 Regions in a Patient with Multiple Congenital Anomalies, Congenital Hypothyroidism and Adrenogenital Syndrome
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Abstract PDF
HRP0089P3-P247

A Rare Chromosomal Disorder, Trisomy 4p
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Abstract PDF
HRP0089P3-P248

Prediction of Response to Growth Hormone Treatment in Korean Girls with Turner Syndrome
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Abstract PDF
HRP0089P3-P250

Prader-Willi Patient with Rectal Bleeding - Experience in Center for Rare Endocrine Disordesrs in Varna, Bulagria
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Abstract PDF
HRP0089P3-P251

Mosaicism 47XXX/45X0, a Case Report
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Abstract PDF
HRP0089P3-P252

Factors Influencing the Selection of Injection Areas During Self-therapy for Growth Hormone Therapy Among Patients 10-15 Years Old
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Abstract PDF
HRP0089P3-P253

Tall Stature: A Diagnosis is Sometimes Difficult
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Abstract PDF
HRP0089P3-P254

Woodhouse-Sakati Syndrome: Clinical and Molecular Study on a Qatari Family with C2orf37 Gene Mutation
Direct

Abstract PDF
HRP0089P3-P255

Factors Affecting Height Velocity in Normal Prepubertal Children
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Abstract PDF
HRP0089P3-P256

Low Dose Growth Hormone using IGF1 Dose Titration is Associated with Sustained Optimal Growth in a Child with Both Turner and Down Syndrome
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Abstract PDF
HRP0089P3-P258

Late Referral of Siblings with Combined Pituitary Hormone Deficiency (PROP1)
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Abstract PDF
HRP0089P3-P259

17p13.1 Microduplication Syndrome in a Child with Familial Short Stature and GH Deficiency: A Short Case Report
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Abstract PDF
HRP0089P3-P260

Prader Willi Syndrome: Clinical Profile
Direct

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HRP0089P3-P261

Leri-Weill Syndrome Phenotype with Atypical Cytogenetic Finding
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Abstract PDF
HRP0089P3-P262

Deletion of 12q12 Increases the Risk of Growth Retardation and Intellectual Disability
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Abstract PDF
HRP0089P3-P401

Is Using a Specific Growth Charts a Chance to be More Precise in Evaluation the Growth of the Children and Adolescence with Down Syndrome? Comparison of the Down's Syndrome Growth Charts with the Growth Charts for Polish Population
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Abstract PDF
HRP0089P3-P406

Two Siblings with Prader-Willi Syndrome Caused by Microdeletion Derived from the Paternal Grandmother
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Abstract PDF
HRP0089P3-P415

Case Report: Novel ACAN Mutation in a SGA Short Stature without Accelerated Skeletal Maturation
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Abstract PDF
HRP0089P1-P189

Clinical Features and Assessment of the Pathway-Care Proposed by ISPED-Gsa Study Group in an Pediatric Italian Cohort with Pseudohypoparathyroidism
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Abstract PDF
HRP0089P1-P190

Overview of Leading Causes of Death among French Patients with Prader-Willi Syndrome, 2004-2014
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Abstract PDF
HRP0089P1-P192

Final Adult Height, Insulin-like Growth Factor 1 (IGF-I) Concentration in Adolescents and Young Adults with [beta]-Thalassemia Major (BTM) with and Without Growth Hormone Deficiency
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Abstract PDF
HRP0089P1-P193

McCune-Albright-Syndrome: Clinical and Genetic Study in a Large Cohort of Pediatric Patients
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Abstract PDF
HRP0089P2-P284

Endocrine and Metabolic Complications in Children and Adolescents with Sickle Cell Disease: An Italian Cohort Study
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Abstract PDF
HRP0089P2-P285

Bone Marrow Failure in McCune Albright Syndrome
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HRP0089P2-P286

Final Adult Height, Insulin-Like Growth Factor 1 (IGF-I) Concentration and Endocrine Complications in Adolescents and Young Adults with [beta]-Thalassemia Major (BTM) Who Received Oral Iron Chelation (OIC) in Comparison with Those Who Did Not Use OIC
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HRP0089P2-P287

Endocrine Challenges in Patients with Thalassemia
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HRP0089P2-P288

Can Oral Iron Chelation Therapies Reduce Endocrine Complications in [beta]-Thalassemia Major Patients?
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HRP0089P2-P289

Statural Growth and Endocrinopathies in Relation to Liver Iron Content (LIC) and Insulin-Like Growth Factor 1 (IGF-I) Concentration in Adolescents with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD)
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Abstract PDF
HRP0089P2-P290

Successful Treatment of Severe Atopic Dermatitis with Calcitriol and Paricalcitol in an 8-Year Old Girl
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Abstract PDF
HRP0089P2-P291

Hypoglycemia in Adolescence as the Presenting Sign of Familial MEN1
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Abstract PDF
HRP0089P2-P292

Aldosterone, Renin, Sodium and Potassium Excretion in Normotensive Prepubertal Children
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Abstract PDF
HRP0089P2-P294

British Society for Paediatric Endocrinology and Diabetes Peer Review of Specialised Paediatric Endocrinology Services in the UK - Evaluation of the Process
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Abstract PDF
HRP0089P2-P296

The Impact of Military Conflict in the East of Ukraine on the Physical Development of Children and Adolescents
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Abstract PDF
HRP0089P2-P297

Polycystic Ovary Syndrome Metabolic Syndrome Predisposition in Puberty
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Abstract PDF
HRP0089P2-P298

Fanconi-Bickel Syndrome in Sudanese Children, Case Series
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Abstract PDF
HRP0089P2-P299

The N309K Pro-Protein Convertase Type 1 (PCSK1) Gene Mutation Causes Lack of Spontaneous Puberty and Primary Amenorrhea
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HRP0089P2-P300

Somatostatin Experiment in Prohormone Convertase Deficiency
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Abstract PDF
HRP0089P3-P265

Insulinoma as Initial Presentation of Multiple Endocrine Neoplasia Type 1
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Abstract PDF
HRP0089P3-P266

Assessment of Ovarian Reserve in Young Women with Hashimoto Disease - The Pilot Study
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Abstract PDF
HRP0089P3-P267

Unusual Clinical Presentation of Autoimmune Polyendocrinopathy Type 1
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Abstract PDF
HRP0089P3-P268

Glycemic Abnormalities and Normal Thyroid Function in Adolescent Survivors of Childhood Acute Lymphocytic Leukemia Who Required Repeated Packed Red Cell Transfusion During Treatment
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Abstract PDF
HRP0089P3-P269

Graves' Disease in Children with T1DM: A Report of Three Cases
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Abstract PDF
HRP0089P3-P270

Case Report: Neonatal McCune-Albright Syndrome with Juvenile Ovarian Granulosa Cell Tumor in a 4 Months Old Girl
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HRP0089P3-P271

Polyostotic Fibrous Dysplasia of McCune Albright Syndrome Responding to Intravenous Zoledronate Therapy
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HRP0089P3-P272

Two Cases of Costello Syndrome and Literatures Review
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HRP0089P3-P273

Endocrine Complications in Beta-Thalassaemia Major Children
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HRP0089P3-P274

The Case of Combination of Multinodular Goiter and Sertoli-Leydig Cell Ovarian Tumor due to Mutation in DICER1 Gene
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HRP0089P3-P275

Unusual Case of Autoimmune Polyglandular Syndrome
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HRP0089P3-P276

Autoimmunepolyendocrinopathy-Candidiasis-Ectodermal Dystrophy: A Case Report
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HRP0089P3-P277

Wolman Disease: Long-Term Endocrine and Metabolic Comorbidities
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HRP0089P3-P279

Near Electromagnetic Fields - Induced Syndrome: Unsuspected and Newly Recognised
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HRP0089P3-P280

Polycystic Ovary Syndrome Gene/Gene Products Interaction Network
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Abstract PDF
HRP0089P3-P281

Basal Metabolic Rate as Moderator of Inflammation in PCOS
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Abstract PDF
HRP0089P3-P282

Insight of Differential Diagnosis of DAX-1 from Two Patients with Elevated Testosterone in Early Infancy
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HRP0089P3-P283

Rapid Onset and Progression of Chronic Kidney Disease in a Child with Autoimmune Polyglandular Syndrome Type 1
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HRP0089P3-P405

Lessons from Wolfram Syndrome: Initiation of DDAVP Therapy Causes Renal Salt Wasting due to Elevated ANP Levels, Rescued by Fludrocortisone Treatment
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HRP0089P3-P410

A Novel Detrimental Homozygous Mutation of WFS1 Gene in Two Sisters from Non-consanguineous Parents with Untreated Diabetes Insipidus
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HRP0089P1-P194

A 7-Year Update Report of a National, Interdisciplinary Endeavour to Improve Outcomes for Children and Young People Under 19 Years of Age with Hypothalamic Pituitary Axis Tumours (HPAT) Using Multi-site Video Conferencing
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HRP0089P1-P195

Long Term Reversibility of Presumed ACTH Deficiency (ACTHd) in Children and Young People (CYP) with Intracranial Germ Cell Tumours (IGCT)
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HRP0089P1-P196

Endocrine Follow-up of Children with a History of Brain Tumour: Data from Our Large Cohort at Necker University Hospital, Paris, 2010-2015
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HRP0089P1-P197

A Single Centre Experience of Managing a Series of Childhood Macro/Giant-Prolactinoma
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Abstract PDF
HRP0089P1-P198

A National UK Guideline for Managing Pituitary Adenomas in Children and Young People Under 19 Years Developed According to the AGREE II Framework
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Abstract PDF
HRP0089P1-P200

PROKR2 Mutations in Patients with Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
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HRP0089P1-P201

Anastrozole is Safe as Monotherapy in Early Maturing Girls with Compromised Growth, Further Improving Gain in Predicted Adult Height by the Initial Combination Therapy of an LHRH Analogue and an Aromatase Inhibitor: Results from the 'Gail' Study ISRCTN11469487
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HRP0089P1-P202

Long-acting Octeotride Treatment in Children with Neurofibromatosis Type 1 - Optic Pathway Tumors and Growth Hormone Excess
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HRP0089P1-P203

Serum Concentrations of the Endocrine Disruptors-organochlorine Pesticides (OCPs) in Greek Children with Neurodevelopmental Disorders
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Abstract PDF
HRP0089P1-P205

A Paternally Inherited Familial Precocious Puberty Caused by a Novel MKRN3 Frameshift Variant
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HRP0089P1-P206

MKRN3 Levels in Girls with Central Precocious Puberty During GnRHa Treatment: A Longitudinal Study
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HRP0089P1-P208

Testicular Development and Puberty in Boys with Duchenne Muscular Dystrophy: Results From the ScOT-DMD Study
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HRP0089P1-P209

Exposure to BPA and Phthalates and Timing of Puberty in Girls
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HRP0089P1-P210

Hypothalamic-pituitary-testicular Axis Response to Sub-maximal Aerobic Exercise, in Pre- and Early- Pubertal Normal Weight and Obese Boys
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HRP0089P1-P211

Effect of Pubertal Blockade and Cross-sex Hormone Treatment on the Growth Spurt in Young Transgender Adolescents: A First Report
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HRP0089P1-P212

Real-World Safety Data in a Cohort of Children with Noonan Syndrome Treated with GH: Final Results from NordiNet International Outcome Study (IOS) and ANSWER Program
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HRP0089P2-P301

Efficacy and Safety of Triptorelin 3-Month Formulationin Patients with Central Precocious Puberty and BMI Evaluation.
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HRP0089P2-P302

Triptorelin Test in Idagnosing Central Precocious Puberty
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HRP0089P2-P303

Foot Length Growth is a Novel Marker of Early Puberty
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HRP0089P2-P304

Ultrasound-Based Measurements of Testicular Volume in 6-16 Year Old Boys: Intra- and Inter-Observer Agreement and Comparison with Prader Orchidometry
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HRP0089P2-P307

The Effect of GnRH-Analogue Therapy on the Quality of Life of Patients with Central Precocious Puberty and Their Families
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Abstract PDF
HRP0089P2-P308

A Novel Inactivating Compound Heterozygous Mutation in KISS1R/GPR54: Cases of Three Siblings
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Abstract PDF
HRP0089P2-P309

MKRN3 Gene Mutations in a Cohort of Patients with Central Precocious Puberty
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Abstract PDF
HRP0089P2-P310

Can Basal Levels of Luteinizing Hormone (LH) Replace the GnRH Test in the Diagnosis of Precocious Puberty in Girls?
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Abstract PDF
HRP0089P2-P311

Incidence of Delayed Puberty in Adolescents. A Population-Based Study in a County in Central Sweden
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HRP0089P2-P312

Ultrasound Assessment of Pubertal Breast Development: Intra- and Inter-Observer Agreement
Direct

Abstract PDF
HRP0089P2-P313

Neuroendocrine Consequences of Hypothalamic Hamartoma and their Imaging (MRI) and Surgery Correlates
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Abstract PDF
HRP0089P2-P314

The Start Predictors of Puberty in Boys with Constitutional Delay of Puberty
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Abstract PDF
HRP0089P2-P316

Gonadotropin Levels and Frequency of Testosterone Supplementation in Adolescents with Klinefelter Syndrome
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Abstract PDF
HRP0089P2-P318

SOX3 Gene Duplication Associated with Midline CNS Malformations, Hypopituitarism and Neurodevelopmental Abnormalities: 5 Unrelated Cases
Direct

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HRP0089P2-P319

An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency
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HRP0089P2-P320

Pituitary Stalk Interruption Syndrome (PSIS) is Not a Rare Cause of the Congenital Hypopituitarism
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HRP0089P2-P321

Pallister Hall Syndrome: An Unusual Case of Central Precocious Puberty, Prolonged Vaginal Bleeding, Gelastic Seizures and Polysyndactyly in a 3 Month Old Infant
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Abstract PDF
HRP0089P2-P322

Primary Empty Sella Syndrome and Clnical Endocrine Polymorphisms in Children: a Report of 15 Cases
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HRP0089P2-P323

Growth Hormone Deficiency (GHD) in a Patient with Persistence of the Craniopharyngeal Canal with Cephalocele
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HRP0089P2-P324

Endocrine-Metabolic Characterization of Pediatric Patients with Craniopharyngioma: A Single-centre Cohort study
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HRP0089P2-P325

Growth Hormone (GH) Secreting Pituitary Adenomas in Paediatric Practice: 5 Cases Over 20 Years in a Single Tertiary NeuroEndocrine Centre
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HRP0089P2-P326

Pituitary Adenomas in Children and Adolescents: A Retrospective Single-Centre Analysis
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HRP0089P2-P327

Changes of Body Composition of Male Adolescents with GH Deficiency are Diagnostic During Transition
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Abstract PDF
HRP0089P2-P328

AMH and Inhibin B Level in Girls with Central Precocious Puberty
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Abstract PDF
HRP0089P2-P329

Gender-Related Differences in Etiological Distribution of Organic Causes of Central Precocious Puberty
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HRP0089P2-P330

Final Adult Height in Girls with Idiopathic Central Precocious Puberty Treated with Monthly Leuprorelin Acetate VS Triptorelin Acetate
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HRP0089P2-P331

The Impact of Central Precious Puberty on Health-relatedqualityoflifeand Social, Emotive and Behavioral Competences Among Children Treated with GnRHa
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HRP0089P2-P332

Basal and GnRH Analog-stimulated Peak LH Levels for Diagnosing Girls with Early Phase of Central Precocious Puberty
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HRP0089P2-P333

Determination of Urinary Metabolic Profiles of Children with Central and Peripheral Precocious Puberty
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HRP0089P2-P334

Hypertension During GNRH Analogues Therapy in a 10-year-old Girl
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HRP0089P2-P335

The Effect of Polychlorinobiphenyls on Premature Puberty in Girls
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HRP0089P2-P336

A Novel Mutation in 5'; Untranslation Region of Makorin Ring Finger 3 Gene Associated with the Familial Precocious Puberty
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HRP0089P2-P337

A Case of Testotoxicosis Due to a Constitutive Mutation of the LH Receptor Initially Presented as a Central Precocious Puberty at 3 Years Old
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HRP0089P3-P284

Infant with Osteogenesis Imperfecta and Panhypopituitarism: A Case Report
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HRP0089P3-P285

Panhypopituitarism with Tall Stature Diagnosed in a 20 Years Old Boy
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HRP0089P3-P286

Post-Traumatic Hypopituitarism Caused by Pituitary Stalk Transection
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HRP0089P3-P287

Invasive Macroprolactinoma with Cabergoline Induced Cerebrospinal Fluid Rhinorrhoea in Childhood
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HRP0089P3-P288

Bilateral Optic Nerve Hypoplasia Revealing Septo Optic Dysplasia or De Morsier Syndrome: A Case Report
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HRP0089P3-P290

An Interesting Etiology in Childhood Central Diabetes Insipidus HIBERNOMA
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HRP0089P3-P291

Neonatal Panhypopituitarism with Hypoglycemia, Edema, Inspiratory Stridor and Cholestasis
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HRP0089P3-P292

MRI Changes in Time after Cranial Irradiation, and their Relation with Pituitary Function in Survivors of Childhood Medulloblastoma
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HRP0089P3-P294

Growth Hormone Deficit Associated to Complex Arteriovenous Malformation - Case Report
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HRP0089P3-P296

Analysis of Influencing Factors on Bone Maturation in Girls with Central Precocious Puberty (CPP)
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HRP0089P3-P297

Is Premature Adrenarch Associated with Precocıous Puberty via Kisspeptin?
Direct

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HRP0089P3-P299

A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding
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HRP0089P3-P300

Evaluation of Cases with Pubertal Gynecomastia
Direct

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HRP0089P3-P301

A Case of Central Diabetes Insipidus Developed 4 Years after the Non-CNS-Risk Unifocal Bone Lesion of Langerhans Cell Histiocytosis
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HRP0089P3-P302

Effect of Triptoreline in Patients with Central Precocious Puberty at Children's Hospital 1, Ho Chi Minh City, Vietnam
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HRP0089P3-P303

Morning Basal Luteinizing Hormone, A Good Screening Tool for Diagnosing Central Precocious Puberty
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HRP0089P3-P307

Premature Adrenarche and Pseudohypoparathyroidism - Mechanistically Linked or Coincidence?
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HRP0089P3-P309

GLP-1 Receptor Agonist in a Patient with Craniopharyngioma-Related Obesity
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HRP0089P3-P311

Congenital Hypopituitarism Associated with Complex Cranio-Vertebral Junction Anomalies
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HRP0089P3-P312

Premature Thelarche Followed by Acute Lymphoblastic Leukemia in a 1.5 Year Old Girl
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HRP0089P3-P313

Two Cases of Non-syndromic Congenital Unilateral Hypoplasia in One Family
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HRP0089P3-P314

Klinefelter Syndrome with Ambiguous Genitalia in a Child
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HRP0089P3-P315

The Change in Growth's Velocity in Patients with Premature Puberty Receiving Treatment with Analogues of Lyuliberin
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HRP0089P3-P316

The Efficacy of Treatment in Vietnamese Children with Central Precocious Puberty
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HRP0089P3-P317

The Characteristics of Central Precocious Puberty at Children's Hospital 2 in Vietnam
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HRP0089P3-P318

SIG (Special Interest Group)-ENDOPED/RUTE (Brazil): Seven Years Integrating Pediatric Endocrinology Centers throughout the Country
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HRP0089P3-P319

The Relationship Between Prolactin and Development of Puberty in Girls with Early Breast Development
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HRP0089P3-P320

Central Precocious Puberty Appeared in Infancy Period in a Patient of Sotos Syndrome
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HRP0089P3-P418

Clinical and Endocrinological Manifestations of Partial Ectopic Posterior Pituitary: A New Imaging Entity
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HRP0089P1-P213

Insights in Promoter Transactivation of CBX2 Expression
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HRP0089P1-P214

In Silico and In vitro Studies of Human SRD5A2 Variants in Search for Activating Variants Explaining Androgen Excess Reveal Additional Loss of Function Variants
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HRP0089P1-P215

Mutations Involving Nuclear Receptors and Their Cofactors as a Major Cause of 46,XX DSD
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HRP0089P1-P216

SDgeneMatch, A New Tool to Aid the Identification of the Genetic Causes of DSD
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HRP0089P1-P218

Primary Gonadal Dysgenesis in Male 46,XY Patients with NR5A1 Variants Predominantly Affects Sertoli Cell Function
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HRP0089P1-P219

Evaluation of Genetic Etiology in Patients with 46,XY Disorders of Sex Development: One Center Experience
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HRP0089P1-P220

Pitfalls in the Diagnosis of An Infant with 46,XX DSD with Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency - the Value of Simultaneous Genetic Analysis to the Diagnosis in DSD
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HRP0089P1-P221

High Mobility Group Box 1 (HMGB1) and Insulin-Like Growth Factor Binding Protein-2 (IGFBP-2) are Increased, Insulin Decreased and IL-6 Unchanged in Follicular Fluid (FF) from Polycystic Ovarian Syndrome (PCOS)
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HRP0089P1-P222

A De Novo Missense Mutation in the 4th Zinc Finger of the WT1 Gene Causes 46,XY and 46,XX DSD in Two Sibs
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HRP0089P1-P223

Sex-Differences in Reproductive Hormones During Mini-Puberty in Infants with Normal and Disordered Sex Development
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HRP0089P1-P224

The 'ExternalGenitaliaScore' to Describe External Genitalia in Male and Female Infants: A Europeanmulticenter Validation Study
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HRP0089P1-P225

Living with Clitoromegaly: Aqualitative Interview Study of Parent's Responses to Clitoromegaly in Congenital Adrenal Hyperplasia (CAH) with or Without Appearance Altering Surgery
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HRP0089P1-P226

'You Can Put Ideas into Their Heads': Parental Concerns about Children's Participation in DSD Research
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HRP0089P1-P227

Testosterone Levels in Newborn Boys and Girls Related to Penile Length, Anogenital Distance (AGD) and External Genitalia Score (EGS)
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HRP0089P1-P228

Clinical Factors that Determine Surgical Outcome Following Hypospadias Repair
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HRP0089P1-P229

Prevalence of Hypogonadism in Prepubertal Boys with Cryptrochdism
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HRP0089P1-P230

Testicular Ultrasound Measurements to Stratify Pituitary-Gonadal Hormone References in a Cross-Sectional Norwegian Study of Male Puberty
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HRP0089P1-P231

Altered Vascular Function in Boys with Hypospadias - Role of Reactive Oxygen Species
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HRP0089P1-P232

Gonadectomy for Adults with DSD Conditions in the International Disorders of Sex Development Registry
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HRP0089P1-P233

Phenotypic and Genetic Assessment of Boys with a Suspected XY Disorder of Sex Development
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HRP0089P1-P234

Pediatricians' Attitudes and Beliefs towards Transgender Persons
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HRP0089P1-P235

Diagnosis of Adolescent Polycystic Ovary Syndrome (PCOS) According to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS
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HRP0089P1-P238

Effect of Intrauterine Growth Restriction on Ovarian Follicle Pool
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HRP0089P1-P239

Sustainability of Estradiol Drug Concentrations in Cut Matrix Patches; A Study of Different Brands with Potential Use for Pubertal Induction
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HRP0089P1-P240

Serum Anti-Mullerian Hormone (AMH) concentrations and Reduced Appendix Testis Estrogen Receptor Expression in Cryptorchidism
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HRP0089P1-P241

The Comparisons of the Adult Height Gain and the Menarchal Age of the Girls with Central Precocious Puberty after Gonadotropin Releasing Hormone Agonist Alone and Those Treated with Combined Growth Hormone Therapy
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HRP0089P1-P242

AMH Level of Infants with Premature Thelarche and Possible Relationship between AMH and Mini-puberty
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HRP0089P1-P243

Circulating Makorin Ring Finger Protein 3 Levels Predict Central Precocious Puberty in Girls
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HRP0089P1-P244

Polycystic Ovarian Syndrome in Adolescents: Characterising the Clinical Phenotype and the Role of Precision Medicine
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HRP0089P1-P245

Thyroid Function in Central Precocious Puberty Girls
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HRP0089P1-P246

Clinical Phenotypes and Mutation Spectrum of Patients with Isolated Gonadotropin-Releasing Hormone Deficiency in a Single Academic Center
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HRP0089P2-P338

Physical Assessment in Chinese Children with 5a-reductase Type 2 Deficiency
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HRP0089P2-P339

Results of Exome Sequencing in Disorders of Sex Development
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HRP0089P2-P340

Awareness is The Key: Heavy Delay in Diagnosis of 17-[beta]-Hydroxysteroid-Dehydrogenase III Deficiency (17bHSD3D) and Other Insights and Conclusions from a Cohort of Ten 17bHSD3D Patients in Germany
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HRP0089P2-P341

Evaluation of Three Patients with 46,XY Gonadal Dysgenesis due to Desert Hedgehog Gene Mutations
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HRP0089P2-P342

In-silico Gene-protein Analysis and Clinical Phenotype Characterisation of Three Novel NR5A1/SF1 Gene Mutations Presenting with 46,XY DSD
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HRP0089P2-P343

Clinical, Biochemical, Structural and Functional Characterization of a Novel P450 Oxidoreductase Mutation Causing Virilization in a 46,XX Patient
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HRP0089P2-P344

Copy-Number Variations of the Human Olfactory Receptor Gene Family in Patients with Macromastia and Prepubertal Gynecomastia
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HRP0089P2-P345

Histopathologic Characterization of Patients with 46,XX Testicular and Ovotesticular Disorders of Sex Development
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HRP0089P2-P346

Current Medical Care of Children and Adolescents with Disorders/differences of Sex Development in Switzerland
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HRP0089P2-P347

Clinical, Laboratory and Molecular Genetic Findings of Patients with 17[beta]-Hydroxysteroid Dehydrogenase 3 Deficiency
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HRP0089P2-P348

Revisiting the Diagnosis: Next Generation Sequencing (NGS) Identifies Concurrence of PAIS in a Previously Reported Case of Klinefelter Syndrome (47,XXY) with Hypospadias
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HRP0089P2-P349

A 46,XX Female with WT1 Mutation, Congenital Nephrotic Syndrome and a Complex Disorder of Sex Development
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HRP0089P2-P350

Psychological Gender Features and Social Abilities and in Adolescent Girls - Influence of Obesity and Hyperandrogenism
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HRP0089P2-P351

Two Unrelated Cases of Severe Insulin Resistance Due to Insulin Receptor Mutation Discovered During Adolescence
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Abstract PDF
HRP0089P2-P352

A Systematic Review of Reported Outcomes for Hypospadias
Direct

Abstract PDF
HRP0089P2-P353

Young Transgender People's Attitudes to Fertility Preservation and Practice
Direct

Abstract PDF
HRP0089P2-P354

Etiology of Disorders of Sex Development in Kenyan Children and Adolescents
Direct

Abstract PDF
HRP0089P2-P355

Adiponectin as a Marker of Peripheral Insulin Resistance in Adolescents with Polycystic Ovarian Syndrome (PCOS) and as a Tool to Suspect Insulin Receptor Defects
Direct

Abstract PDF
HRP0089P2-P356

Diagnostic Experiences and Concerns in Adolescents with Polycystic Ovary Syndrome
Direct

Abstract PDF
HRP0089P2-P357

Impact of Hydrocortisone Treatment on Clitoral Size During First Year of Life in Girls with Congenital Adrenal Hyperplasia (CAH)
Direct

Abstract PDF
HRP0089P2-P358

Persistent Mullerian Duct Syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys
Direct

Abstract PDF
HRP0089P2-P359

Clinical, Hormonal and Metabolic Profile in Adolescent Girls Treated with Gonadotropin Releasing Hormone Agonist for Idiopathic Central Precocious Puberty
Direct

Abstract PDF
HRP0089P2-P360

Spontaneous Pregnancies in Female Survivors of Childhood Hematological Malignancies Post Allogeneic Haemopoietic Stem Cell Transplantation
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Abstract PDF
HRP0089P2-P361

Towards an Integrated Approach to Diagnosis of 46,XY Disorder of Sex Development
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Abstract PDF
HRP0089P2-P363

The Human Genital Tubercle is Steroidogenic Organ at Earlypregnancy
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Abstract PDF
HRP0089P2-P364

Transgender Medicine is a Significant Part of Paediatric Endocrinology
Direct

Abstract PDF
HRP0089P2-P365

Prospective Investigation of the Influence of Triptorelin Treatment on Body Weight and Body Mass Index of Girls Who Were Diagnosed with Idiopathic Precocious Puberty or Early Puberty
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Abstract PDF
HRP0089P2-P366

Genetic Etiologies and Gender Outcomes of Patients with Disorders of Sex Development Presenting with Asymmetric Gonads
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Abstract PDF
HRP0089P2-P367

A Rare Form of Ovotesticular DSD: Diagnostic and Management Challenges
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Abstract PDF
HRP0089P2-P368

A Case of Gonadal Dysgenesis Due to a Novel Homozygous Mutation in NR5A2 Gene
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Abstract PDF
HRP0089P2-P369

Assessment of Initial Investigation Requested in Adolescents with Menstrual Disorders
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Abstract PDF
HRP0089P2-P370

Persistent Mullerian Duct Syndrome in Twin Brothers Caused by a Novel Mutation in the AMHR2 Gene
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Abstract PDF
HRP0089P2-P371

No Difference in Cognitive Performance or Gender Role Behaviour in Men with and without Hypospadias
Direct

Abstract PDF
HRP0089P2-P372

Assessment of the Gonadotrophin-Gonadal Axis and Sertoli Cell Function in Partial Androgen Insensitivity Syndrome
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Abstract PDF
HRP0089P2-P374

Evaluation of Serum Anti-Mullerian Hormone and Androstenedione Levels in Adolescents Girls with Menstrual Irregularities
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Abstract PDF
HRP0089P2-P375

Could Basal AMH Replace hCG Stimulation Test in XY Disorder of Sex Development Cases
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Abstract PDF
HRP0089P3-P321

Gonadal Tumor Incidence in Patients with Disorders of Sex Development Containing Y Chromosome or Y-derived Sequences - Experience from One Clinical Center
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Abstract PDF
HRP0089P3-P322

New Method of Surgical Correction of Female Hypospadias in Girls with Disorders of Sex Development and Stenosis of Artificial Introitus
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Abstract PDF
HRP0089P3-P324

Challenges in Managing 46, XY Partial Gonadal Dysgenesis in Saudi Arabia
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Abstract PDF
HRP0089P3-P325

A Paternally Inherited NR5A1 Mutation in a Case of 46,XY Partial Gonadal Dysgenesis
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Abstract PDF
HRP0089P3-P326

Clinical Presentation and Characteristics of DSD in Kenyan Children and Adolescents
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Abstract PDF
HRP0089P3-P327

Evolutive Profile of Pauci-symptomatic Forms of Mc Cune Albright Syndrome
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Abstract PDF
HRP0089P3-P328

A 45X0/46XY Girl Diagnosed with Prepubertal FSH Elevation
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Abstract PDF
HRP0089P3-P329

About a Case of Leydig Cell Tumor Associated with Central Precocious Puberty
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Abstract PDF
HRP0089P3-P330

Gender Dysphoria
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HRP0089P3-P331

GnRH Analogues and Cross-Sex Hormonal therapy: Side Effects in Transgender Youth
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Abstract PDF
HRP0089P3-P332

Klinefelter Syndrome with Low Gonadotropin Levels
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Abstract PDF
HRP0089P3-P333

Young Male Adolescent with Gender Dysphoria (GD)/Gender Incongruence - A Case Presentation
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Abstract PDF
HRP0089P3-P334

Effect of Gonadotropin-Releasing Hormone Agonist Treatment in Boys with Central Precocious Puberty and Early Puberty
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Abstract PDF
HRP0089P3-P335

DSD in Ukraine: Our Experience
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Abstract PDF
HRP0089P3-P336

A Turkish Family with 46,XY Disorder of Sex Development Due to 17b-Hydroxysteroid Dehydrogenase Type 3 Deficiency
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HRP0089P3-P337

Normal External Genitalia in a Female with Classic, Salt-Wasting 21-Hydroxylase Deficiency
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HRP0089P3-P338

Ovarian Leydig Cell Tumor in an 8 Years Old Girl Misdiagnosed as Congenital Adrenal Hyperplasia Due to Elevated 17-Hydroxi-Progesterone
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HRP0089P3-P339

Analysis of Genetic Mutations in a Chinese Pedigree Affected with Idiopathic Hypogonadotropic Hypogonadism Syndrome
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HRP0089P3-P341

Cytogenetic Spectrum of Ovotesticular Disorder of Sex Development in Egyptian DSD Patients
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HRP0089P3-P343

Genital Abnormalities and Management Outcomes as Seen in the University of Port Harcourt Teaching Hospital
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HRP0089P3-P344

A Case Report: A Girl with 46,XY Karyotype and Disorder of Androgen Synthesis
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HRP0089P3-P345

The Positive Effect of the Low-Dose Contraceptive on the Course of Cystic Fibrosis in the Adolescent Female
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HRP0089P3-P346

Ovotesticular Disorder of Sexual Development: 31 Cases Followed-up in a Single-Center in Brazil
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HRP0089P3-P347

Genital Swelling and Ovarian Stimulation Syndrome in an Extremely Preterm Infant
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HRP0089P3-P348

Significant Penile Growth with Local DHT-Gel in an Infant with 17-Beta HSD-Deficiency
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Abstract PDF
HRP0089P3-P349

Mother and Baby Diagnosed Noonan Syndrome with Dysmorphic Findings
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Abstract PDF
HRP0089P3-P351

A Case Report of Spironolactone Treatment for Becker's Nevus Associated Ipsilateral Breast Hypoplasia
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Abstract PDF
HRP0089P3-P352

New Mutation in 5-Alpha-Redoctase: A Five-Month-Old Infant with a Karyotype of 46 XY
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Abstract PDF
HRP0089P3-P353

A Novel Compound Heterozygous Mutation in CYP19A1 Resulting in Aromatase Deficiency with Normal Gonadotropin Levels and Ovarian Tissue
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Abstract PDF
HRP0089P3-P354

Emblematic Case CAH
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Abstract PDF
HRP0089P3-P355

The Republic of Colombia Has a Constitutional Jurisprudential Precedent Identified as T622 of 2014,1 This Sentence Reaffirms the Importance of the Accurate Diagnosis of Intersexual Patients and Updates How the State Looks at Them2
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Abstract PDF
HRP0089P3-P356

Paediatric Doctors' Experience and Knowledge of the Initial Management of Neonatal Ambiguous Genitalia
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Abstract PDF
HRP0089P3-P357

A Case of Transverse Testicular Ectopia with Persistant Mullerian Duct Syndrome: A Novel AMH Gene Mutation
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Abstract PDF
HRP0089P3-P358

Argentinean First Experience with Transgender Children and Youths
Direct

Abstract PDF
HRP0089P3-P359

Long-Term Follow-up in a Chinese Child with Lipoid Congenital Adrenal Hyperplasiadue to STARmutation
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Abstract PDF
HRP0089P3-P400

Clinical and Molecular Characterization of One Nr5a1 Gene Mutation Found in a Patient WITH 46, XY DSD
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Abstract PDF
HRP0089P3-P408

Genetic Testing by SNP Array Analysis in A Group of Romanian Patients with Disorders of Sexual Development
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Abstract PDF
HRP0089P3-P409

A Novel Gene Mutation and Atypical Clinical Phenotype of Kallmann Syndrome
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Abstract PDF
HRP0089P1-P248

Early Determinants of Thyroid Function Outcome in Children with Congenital Hypothyroidism and a Normally Located Thyroid Gland: A Regional Cohort Study
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Abstract PDF
HRP0089P1-P250

Thyroid Scintigraphy in the Diagnosis of Congenital Hypothyroidism
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Abstract PDF
HRP0089P1-P251

Congenital Hypothyroidism (CH) with Delayed TSH Elevation: The Importance of The Second-Screening Strategy and the Evolution of CH in Preterm Infants
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Abstract PDF
HRP0089P1-P252

Morning Versus Bedtime Levothyroxine Administration: What is the Choice of Children?
Direct

Abstract PDF
HRP0089P1-P253

Long Term Comparison between Liquid and Tablet Formulations of L-Thyroxine (L-T4) in the Treatment of Congenital Hypothyroidism (CH)
Direct

Abstract PDF
HRP0089P1-P254

Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene
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HRP0089P1-P255

Patterns of Thyroglobulin Levels in Infants Referred With High TSH on Newborn Screening, Compared with Iodine-sufficient Healthy Controls
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Abstract PDF
HRP0089P1-P257

Results of the hTPO Mutational Screening in Bulgarian Patients with Congenital Hypothyroidism (CH)
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Abstract PDF
HRP0089P1-P259

A Novel Mutation of IGSF1 Gene
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Abstract PDF
HRP0089P1-P260

Multinodular Goiter in Childhood: A Diagnostic Gateway for Screening DICER1 Syndrome
Direct

Abstract PDF
HRP0089P1-P261

A Novel DICER1 Mutation Identified in a Family with the Multinodular Goiter of Children
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Abstract PDF
HRP0089P1-P263

Expression of ZnT8 Transporter in Thyroid Tissues from Patients with Immune and Non-Immune Thyroid Diseases
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Abstract PDF
HRP0089P1-P265

HLA Alleles and Amino Acid Variants of HLA-A, -B, -C, -DRB1, -DQB1, -DPB1 Molecules in Early-Onset Autoimmune Thyroid Disease
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Abstract PDF
HRP0089P1-P266

Childhood Thyroid Autoimmunity and Relation to Islet Autoantibodies in Children at Risk for Type 1 Diabetes
Direct

Abstract PDF
HRP0089P1-P267

Evaluation of Serum Concentrations of Selected Cytokines OPG and sRANKL in the Diagnosis of Autoimmune Thyroid Disease in Children
Direct

Abstract PDF
HRP0089P1-P268

Analysis of Zinc-Transporter ZnT8 Autoantibodies in Children and Adolescents with Autoimmune Thyroid Diseases
Direct

Abstract PDF
HRP0089P1-P269

The Association between TSHR, IFIH1 and ETV5 Polymorphisms with Graves' Disease and Diabetes Mellitus Type 1 in Children
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Abstract PDF
HRP0089P2-P376

Long Term Monitoring of Graves Disease in Children and Adolescents: Single Center Experience
Direct

Abstract PDF
HRP0089P2-P377

Effects of Thyroid Autoimmunity on Non-Alcoholic Fatty Liver Disease in Euthyroid Girls with Hashimoto's Thyroiditis
Direct

Abstract PDF
HRP0089P2-P378

The Prevalence of Clinically Significant Anti-TPO Positivity in Children with HLA-Conferred Susceptibility to Type 1 Diabetes
Direct

Abstract PDF
HRP0089P2-P379

Encephalopathy Associated with Autoimmune Thyroid Disease: A Case Report
Direct

Abstract PDF
HRP0089P2-P380

Celiac Disease Screening Should be Routinely Offered in Pediatric Population with Autoimmune Thyroid Disease
Direct

Abstract PDF
HRP0089P2-P381

Autoimmune Thyroiditis in Klippel-Feil Syndrome with Arnold Chiari and Syringomyelia
Direct

Abstract PDF
HRP0089P2-P382

Neonatal Monitoring of Newborns Born from Mothers with Graves' Disease: Results of a Retrospective Monocentric Study
Direct

Abstract PDF
HRP0089P2-P384

Graves's Disease During Pregnancy: The Impact on the Fetus and the Newborn
Direct

Abstract PDF
HRP0089P2-P385

Thyroid Hormone Receptor [beta] (THRB) Mutation: Two New Cases of Heterozygous Mutation with Significant Family History
Direct

Abstract PDF
HRP0089P2-P386

Triac Treatment Response to Thyroid Hormone Resistantance
Direct

Abstract PDF
HRP0089P2-P387

Phenotype and Genotype of Four Patients with Thyroid Hormone Resistance Syndrome due to Mutations in the THRB Gene
Direct

Abstract PDF
HRP0089P2-P388

Clinical Course in a Girl with Two hTPO Mutations - Homozygous c.1268G>A (p.Gly393Arg) and Heterozygous c.208C>G (p.Ala70Pro): 27 Years of Follow Up
Direct

Abstract PDF
HRP0089P2-P389

A Neurological Disease Mimicking Central Hypothyroidism: MCT8 Deficiency
Direct

Abstract PDF
HRP0089P2-P390

Multinodular Goiter in Childhood: Look for DICER1 Mutation
Direct

Abstract PDF
HRP0089P2-P391

Application of Elastography in Assesment of Different Benign Thyroid Lesions in Children and Adolescents
Direct

Abstract PDF
HRP0089P2-P392

Clinical Characteristics and Predictive Factors for the Detection of Thyroid Cancer in Children with Thyroid Nodules
Direct

Abstract PDF
HRP0089P2-P393

Thyroid Nodules in Prader-Willi Syndrome
Direct

Abstract PDF
HRP0089P2-P394

Early Medullary Thyroid Carcinoma (MTC) in an Infant with Multiple Endocrine Neoplasia Type 2B (MEN2B, RETS Mutation codon 891)
Direct

Abstract PDF
HRP0089P2-P395

Serum Level of Biotin Rather than the Daily Dose is the Main Determinant of the Interference on Thyroid Function Assays in Patients with Biotinidase Deficiency
Direct

Abstract PDF
HRP0089P2-P396

Thyroid Function Tests and Affecting Factors in Twins and Triplets
Direct

Abstract PDF
HRP0089P2-P397

Hypothyroidism in a Child During Treatment with Nivolumab for a Glioblastoma
Direct

Abstract PDF
HRP0089P2-P398

Diagnosis and Clinical Course of Amiodarone Induced Hyperthyroidism in Three Adolescent Patients
Direct

Abstract PDF
HRP0089P2-P399

Allogenic Bone Marrow Transplantation in Children: Effect on Thyroid Function
Direct

Abstract PDF
HRP0089P2-P400

Follow-up in Children with Non-obese and Non-autoimmune Subclinical Hypothyroidism
Direct

Abstract PDF
HRP0089P2-P401

Clinical Management of Childhood Hyperthyroidism: A Longitudinal Study at a Single Center
Direct

Abstract PDF
HRP0089P2-P402

Association of Thyroid Stimulating Hormone and Free Thyroxine with Cardiometabolic Risk Factors in Euthyroid Korean children and Adolescents Aged 10-18 Years: The Korean National Health and Nutrition Examination Survey 2015
Direct

Abstract PDF
HRP0089P2-P403

Asymptomatic Hyperthyrotropinaemia in Children, Does it Correlate to true Thyroid Gland Dysfunction?
Direct

Abstract PDF
HRP0089P2-P407

Bannayan-Riley-Ruvalcaba Syndrome with PTEN Mutation in a Patient Affected by Congenital Hypothyroidism due to TPO Gene Alteration
Direct

Abstract PDF
HRP0089P2-P409

Do Insulin Like Growth Factors also Influence Growth in Children with Congenital Hypothyroidism: A Cohort Analysis
Direct

Abstract PDF
HRP0089P2-P410

Study of Hearing Function in Children with Congenital Hypothyroidism Attending Alexandria University Children's Hospital
Direct

Abstract PDF
HRP0089P2-P411

Awareness of the Risks of Acquired Iodine Deficiency in Strict Vegan Diets
Direct

Abstract PDF
HRP0089P2-P412

Thyroid Function in the Korean Obese Children and Adolescents: Korea National Health and Nutrition Examination Survey 2013 to 2015
Direct

Abstract PDF
HRP0089P3-P362

Graves' Disease in a Pediatric Population: Results from the Last 17 Years at a Pediatric Endocrinology Unit
Direct

Abstract PDF
HRP0089P3-P363

Acquired Severe Hypothyroidism in Children - Forgotten or Unbelievable Diagnosis in a Time of Large and Easy Availability of Thyroid Tests?
Direct

Abstract PDF
HRP0089P3-P364

Thyroid Disorders and Autoimmunity in Children and Adolescents with Type 1 (T1DM) and Type 2 Diabetes Mellitus (T2DM)
Direct

Abstract PDF
HRP0089P3-P365

The Reference and Follow-up Signs and Symptoms of the Cases Who Are Diagnosed As Hyperthyroidism
Direct

Abstract PDF
HRP0089P3-P366

Clinical Features in Childhood Graves' Disease
Direct

Abstract PDF
HRP0089P3-P367

General Characteristics of Autoimmune Thyroid Diseases and Evaluation of Accompanied Morbiditis
Direct

Abstract PDF
HRP0089P3-P368

Amiodarone Induced Hyperthyroidism in a Pediatric Patient
Direct

Abstract PDF
HRP0089P3-P370

Thyroid Carcinoma in Children: 7 Years' Experience of a Single Center
Direct

Abstract PDF
HRP0089P3-P371

Autoimmune Thyroiditis (Hashimoto Thyroiditis) in a Known Case of Autoimmune Hemolytic Anemia
Direct

Abstract PDF
HRP0089P3-P376

An Impressive Recovery of Arrested Growth and Puberty in a 13 Year Old Boy after Being Treated for Simultaneously Diagnosed Severe Hypothyroidism and Coeliac Disease
Direct

Abstract PDF
HRP0089P3-P377

A Very Rare Thyroid Hormone Resistance Case Having Heterozygous Mutation in THRB Genes
Direct

Abstract PDF
HRP0089P3-P378

Clinical Case (Children's Endocrinology)
Direct

Abstract PDF
HRP0089P3-P379

Thyroid Imaging Study for the Diagnosis of Congenital Hypothyroidism with Thyroid Dysgenesis
Direct

Abstract PDF
HRP0089P3-P380

A Case of Permanent Congenital Hypothyroidism with Compound Heterozygous Mutations in the DUOX2 Gene
Direct

Abstract PDF
HRP0089P3-P381

Growth Catch-up on Acquired Hypothyroidism Presenting with Growth Delay
Direct

Abstract PDF
HRP0089P3-P382

Thyroid Disease in Children and Adolescences with Down Syndrome- 16 Years of Follow Up in a Single Service
Direct

Abstract PDF
HRP0089P3-P383

Corticosteroid Resistant Immune Thrombocytopenic Purpura, is it a Marker of Future Graves Disease?
Direct

Abstract PDF
HRP0089P3-P384

Neonatal Hypothyroidism following Transplacental Amiodarone Treatment for Supraventricular Tachyarrhythmia
Direct

Abstract PDF
HRP0089P3-P385

Rare Case Report of Thyroiditis De Quervain in a Six Years Old Girl
Direct

Abstract PDF
HRP0089P3-P386

Papillary Thyroid Carcinoma in a 7 Year Old Boy Presenting with a Goiter Without Microcalcifications and Enlarged Cervical Lymph Nodes
Direct

Abstract PDF
HRP0089P3-P387

Graves' Disease, Methimazole and SLE-like Reaction:A Case Report
Direct

Abstract PDF
HRP0089P3-P388

A Rare Case of Pediatric Hyperthyroidism
Direct

Abstract PDF
HRP0089P3-P389

Allan-Herndon-Dudley Syndrome in a Patient with Global Delay Development - a Case Report
Direct

Abstract PDF
HRP0089P3-P391

Levothyroxine Treatment of Subclinical (SH) and Overt (OH) Hypothyroidism in Children with Autoimmune Hashimoto Thyroiditis (AHT): A Retrospective Study in Regard with TSH and Free T4 (FT4) at Diagnosis
Direct

Abstract PDF
HRP0089P3-P392

Hashitoxicosis:a Rare Diagnosis in Childhood
Direct

Abstract PDF
HRP0089P3-P393

An Assay Led Astray: A Curious Case of Biotin-Induced Hyperthyroidism
Direct

Abstract PDF
HRP0089P3-P394

A Case of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis (SREAT) in a Girl with Newly Diagnosed Hashimoto Thyroiditis
Direct

Abstract PDF
HRP0089P3-P395

Intellectual Outcome at Childhood in Congenital Hypothyroidism According to Etiology and Treatment Related Factors
Direct

Abstract PDF
HRP0089P3-P397

Head Circumference, Birth Length, and Weight of Neonates of Mothers with Hypothyroidism
Direct

Abstract PDF
HRP0089LB-P3

Glycemic Impact of Long Term Use of Diazoxide Choline Controlled-Release Tablets in Patients with Prader-Willi Syndrome or with Very High Triglycerides
Direct

Abstract PDF
HRP0089LB-P4

An Updated Evolutionary Study in Glucocorticoid Receptors; Insights from a Comprehensive Phylogenetic, SNP's and Mutation's Analysis of the Nuclear Receptors Family: An Updated Evolutionary Study in Glucocorticoid Receptors; Insights from a Comprehensive Phylogenetic, SNP's and Mutation's Analysis of the Nuclear Receptors Family
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Abstract PDF
HRP0089LB-P5

Association between the Use of Antenatal Steroids for Lung Maturation and Hypoglycemia in Newborns Between 26 and 34 6/7 Weeks of Gestation
Direct

Abstract PDF
HRP0089LB-P6

Sex Hormone Levels in Young Children: a Pilot Study of the Japan Environment and Children's Study
Direct

Abstract PDF
HRP0089LB-P7

Mutational Analysis of SRD5A2 and AR Genes in Indian Children with 46 XY Disorders of Sex Development
Direct

Abstract PDF
HRP0089LB-P8

Pharmacokinetics of Diazoxide Choline Controlled-Release Tablets, a Once Daily Treatment Being Evaluation in Patients with Prader Willi Syndrome
Direct

Abstract PDF
HRP0089LB-P9

Two Siblings with Autosomal Recessive Syndromic Hypopituitarism Caused By Mutations in TBC1D32
Direct

Abstract PDF
HRP0089LB-P10

The Influence of Oil-Soluble Iodinated Contrast Medium (Lipiodol) on Child's Thyroid Function in Mice
Direct

Abstract PDF
HRP0089LB-P11

Metabolic Profile in Survivors of Pediatric Hematopoietic Stem Cells Transplantation after Chemotherapy-Only Conditioning
Direct

Abstract PDF
HRP0089LB-P12

Disrupting the Norm: The Experience of Young People with DSD
Direct

Abstract PDF
HRP0089LB-P13

Clinical and Endocrine Characteristics and Genetic Analysis of Korean Children with McCune-Albright Syndrome
Direct

Abstract PDF
HRP0089LB-P14

Beta-cell Function in Chinese Youngsters with Type 1 Diabetes and Assessment of Surrogate Markers of Severe Insulin Deficiency
Direct

Abstract PDF
HRP0089LB-P16

Successful Treatment of Alopecia Totalis with Calcitriol and Paricalcitol in Two Girls Aged 3 and 7-Years
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Abstract PDF
HRP0089LB-P17

Protein-Induced Hypoglycemia Secondary to Hyperinsulinism-Hyperammonemia (HI/HA) Syndrome: A GLUD1 Gene Mutation
Direct

Abstract PDF
HRP0089LB-P19

Characterization and Clinical Course of Prolactinoma in Korean Adolescents
Direct

Abstract PDF
HRP0089LB-P20

The Efficacy and Safety of Octreotide Treatment for Diazoxide-Unresponsive Congenital Hyperinsulinism in China
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Abstract PDF

ESPE Abstracts

57th Annual ESPE (ESPE 2018)

EPosters

BiosciAbstracts