ePosters | 0086 | ESPE2016 | 55th Annual ESPE

Scientific Programme, ePosters & Abstracts

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55th Annual ESPE

Paris, France
10 Sep 2016 - 12 Sep 2016

Paris, France: 10-12 September 2016 Further information

HRP0086RFC1.1

Tracing the Glucocorticoid Receptor Evolutionary Pedigree: Insights from a Comprehensive Phylogenetic Analysis of the Full NR Super-Family
Direct

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HRP0086RFC1.2

Glucocorticoid Deficiency Due to Disruption of Mitochondrial Steroidogenesis Leads to Dysregulation of Antioxidant Pathways and Nucleotide Biosynthesis
Direct

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HRP0086RFC1.3

Impaired Cardiac Function in a Mouse Model of Generalized Glucocorticoid Resistance
Direct

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HRP0086RFC1.4

Mutations of ABCD1 in 16 Vietnamese Patients with X-linked Adrenoleukodystrophy
Direct

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HRP0086RFC1.5

A Novel Animal Model to Study 21-Hydroxylase Deficiency in vivo
Direct

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HRP0086RFC1.6

Pediatric Patients with Congenital Adrenal Hyperplasia have Unfavorable Changes in their Cardiovascular Risk Profile
Direct

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HRP0086RFC1.7

The Recovery of Adrenal Function in Children with Chronic Asthma Assessed by Low Dose Short Synacthen Test (LDSST)
Direct

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HRP0086RFC1.8

Adrenal Dysfunction in HIV-Exposed Uninfected Infants Receiving Ritonavir-Boosted Lopinavir, an HIV Protease Inhibitor, for the Prevention of Breastfeeding HIV Transmission. An ANRS 12174 Substudy
Direct

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HRP0086RFC2.1

25-OH-Vitamin D Status in a Pediatric Population of Subjects Affected By Prader-Willi Syndrome Compared to Matched Obese Controls
Direct

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HRP0086RFC2.4

Results of Orthopaedic Surgery in Children with X-Linked Hypophosphatemic Rickets (XLHR)
Direct

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HRP0086RFC2.5

Growth Patterns and Fractures in Boys with Duchenne Muscular Dystrophy: Insights from Over 800 Boys in the UK North Star Cohort
Direct

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HRP0086RFC2.6

Combining COLD and MAMA-PCR Real Time Taqman Tecniques to Detect and Quantify the R201 GNAS Mutation Causing McCune-Albright Syndrome
Direct

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HRP0086RFC2.7

Effect of Paternal Loss-of-Function Mutations of GNAS on Growth During the Childhood: A Role for XL
Direct

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HRP0086RFC2.8

Final Heights and BMI in Patients Affected with Different Types of Pseudohypoparathyroidism
Direct

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HRP0086RFC3.1

Endocrinopathy in Childhood Intracranial Germ Cell Tumours is Predicted by Disease Location not Treatment: 30 year Experience from a Single Tertiary Centre
Direct

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HRP0086RFC3.2

Subfertility After Chemotherapy in PNET Tumours: 34 year Experience from a Single Centre (1980-2013)
Direct

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HRP0086RFC3.3

Unraveling the Link between Optic Nerve Hypoplasia and Pituitary Hormone Dysfunction
Direct

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HRP0086RFC3.4

Children and Adolescents with Severe TBI can Develop Late Pituitary Dysfunction Independently of the Results of the First Pituitary Evaluation
Direct

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HRP0086RFC3.5

Prospective Dynamic Evaluation of Hypothalamo-Pituitary Function in 30 Cases of Paediatric Craniopharyngioma, by Hypothalamic Injury and Treatment; A Single Centre Series
Direct

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HRP0086RFC3.6

Priority Target Conditions of Growth-Monitoring in Children: Toward Consensus
Direct

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HRP0086RFC3.7

Pituitary Structural Abnormalities in Idiopathic Isolated Growth Hormone Deficiency
Direct

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HRP0086RFC3.8

Anthropometric and Endocrine Features in Children and Adolescents with Type 1 Narcolepsy
Direct

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HRP0086RFC4.2

Adipocytokines Delay Pubertal Maturation of Human Sertoli Cells
Direct

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HRP0086RFC4.3

Early Growth Patterns are Associated with Alterations in Adipocytokine Levels and Fat Distribution Measured by DXA in 982 Children/Adolescents
Direct

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HRP0086RFC4.4

Metabolic Syndrome Markers Correlate with Gut Microbiome Activity in Children Born Very Preterm
Direct

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HRP0086RFC4.5

Steroid Metabolomic Signature of Liver Disease in Childhood Obesity
Direct

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HRP0086RFC4.6

Adipose Tissue - A Source of Hyperandrogenism in Obese Females?
Direct

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HRP0086RFC4.7

Prevalence and Characterization of Retinal Alterations in a Cohort of Overweight and Obese Children
Direct

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HRP0086RFC5.1

Adiponectin and Leptin in Children with Type 1 Diabetes for 3-5 years with or without Residual [beta] cell Function
Direct

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HRP0086RFC5.2

Limits of Agreement between HbA1c Levels Measured in Different Laboratories Following the Introduction of the International Federation of Clinical Chemistry and Laboratory Medicine Standardised Values
Direct

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HRP0086RFC5.3

Sexual Lifestyle among Young Adults with Type 1 Diabetes
Direct

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HRP0086RFC5.4

[ldquo]Transient[rdquo] Neonatal Diabetes In Adulthood: Metabolic Outcomes
Direct

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HRP0086RFC5.5

The Efficacy of Insulin Degludec in Children and Adolescents with Type 1 Diabetes
Direct

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HRP0086RFC5.6

Clinical Management of the Mitchell-Riley Syndrome Due to RFX6 Gene Mutations: Aggressive Support Results in Improved Outcome
Direct

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HRP0086RFC5.7

Early Successful Hematopoietic Cell Transplantation (HSCT) in a Boy with IPEX Syndrome Caused by Novel C.721T>C FOXP3 Mutation
Direct

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HRP0086RFC5.8

Stress Management and Health Promotion through Family Intervention Improves Metabolic Control in Children and Adolescents with Type 1 Diabetes
Direct

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HRP0086RFC6.2

RAB3IP and DGCR8 as a Potentially Pathogenic Novel Candidate Gene Involving in Growth Disorders
Direct

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HRP0086RFC6.3

Effect of Very Early Growth Hormone (GH) Treatment on Long-term Growth in Girls with Turner Syndrome (TS): A Multicenter, Open-Label, Extension Study
Direct

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HRP0086RFC6.4

Growth Hormone (GH) Treatment in Skeletal Dysplasias - Short-term Results in Prepubertal Children Reported in KIGS
Direct

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HRP0086RFC6.5

Abnormal Videofluoroscopic Swallow Studies (VFSS) in Infants with Prader-Willi Syndrome Indicate a High Rate of Silent Aspiration
Direct

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HRP0086RFC6.6

Growth Hormone (GH) Deficiency Type II: Clinical and Molecular Evidence of Impaired Regulated GH Secretion Due to an Gln181Arg GH-1 Gene Mutation
Direct

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HRP0086RFC6.7

Characteristics of Responders and Poor-responders to Increlex® Therapy - Data from Children Enrolled in the European Increlex® Growth Forum Database (EU-IGFD)
Direct

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HRP0086RFC6.8

The Actual Incidence of Small for Gestational Age (SGA) Newborns and their Catch-up Growth is Dramatically Lower than Previously Considered
Direct

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HRP0086RFC7.1

Tissue Engineered Collagen Based Tubular Scaffolds for Urethral Regeneration. A Novel Technology for the Surgical Treatment of VSD (Variation of Sex Development) Patients with Severe Hypospadias
Direct

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HRP0086RFC7.2

Reference Values for External Genitalia Size and Steroid Hormone Levels in Female Neonates
Direct

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HRP0086RFC7.3

Harmonisation of Serum Dihydrotestosterone Analysis: Establishment of an External Quality Assurance Program
Direct

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HRP0086RFC7.4

A Mutation in WT1 (Wilms' Tumor Suppressor 1) Associated with 46,XX TDSD
Direct

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HRP0086RFC7.5

Fertility Preservation in an Adolescent Boy: Inducing Puberty and Spermatogenesis Prior to Bone Marrow Transplantation
Direct

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HRP0086RFC7.6

The Hopeful Beginnings of Fertility Preservation in Children
Direct

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HRP0086RFC7.7

Clinical Decision-Making in Disorders of Sex Development (DSD): Physician Recommendations Pre- and Post-Consensus Statement
Direct

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HRP0086RFC7.8

Premature Adrenarche in Girls at Pubertal Onset is Associated with High Androgens, but Lower AMH Concentrations
Direct

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HRP0086RFC8.1

Somavaratan (VRS-317) Treatment of Children with Growth Hormone Deficiency (GHD): Results at 2 Years (NCT02068521)
Direct

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HRP0086RFC8.2

Pharmacokinetic Modelling Predicts Native hGH Levels Following Administration of a Sustained-Release Prodrug, TransCon hGH, to Children with GHD
Direct

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HRP0086RFC8.3

Batch-to-Batch Consistency of a Highly O-Glycosylated Long-Acting Human Growth Hormone (MOD-4023)
Direct

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HRP0086RFC8.4

A Hybrid Fc-fused Human Growth Hormone, GX-H9, Shows a Potential for Weekly and Semi-monthly Administration in Clinical Studies
Direct

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HRP0086RFC8.5

Optimal Sampling of IGF-1 During Weekly Administration of a Long Acting Human Growth Hormone (MOD 4023)
Direct

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HRP0086RFC8.6

A Six-Month Safety and Efficacy Study of TransCon hGH Compared to Daily hGH in Pre-Pubertal Children with Growth Hormone Deficiency (GHD)
Direct

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HRP0086RFC8.7

Safety and Tolerability of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): 24-month Complete Dataset Results of a Phase 2 Study in Children with Growth Hormone Deficiency
Direct

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HRP0086RFC8.8

Efficacy of Once-Weekly Administration of CTP-Modified Human Growth Hormone (MOD-4023): 24-month Complete Database Results of a Phase 2 Study in Children with Growth Hormone Deficiency
Direct

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HRP0086RFC9.1

Neonatal Diabetes due to NKX2.2 Mutation - Genotype, Clinical Phenotype and Therapeutic Challenges in a Very Low Birth Weight Diabetic Neonate
Direct

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HRP0086RFC9.2

Missense Mutation of GLIS3 Gene Resulting in Neonatal Diabetes and Congenital Hypothyroidism
Direct

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HRP0086RFC9.3

Molecular Analysis of a Large Cohort of MODY Patients by Next Generation Sequencing
Direct

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HRP0086RFC9.4

Prevalence of Monogenic Diabetes in the Lithuanian Pediatric and Young Adult Population
Direct

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HRP0086RFC9.5

Non-Mody Monogenic Diabetes: A Very Heterogenous and Problematic Group of Diabetes
Direct

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HRP0086RFC9.6

Emerging Pitfalls of Etiological Diagnosis of Diabetes in Children and Adolescents? Analysis of a French Cohort of 310 Recent-Onset Cases
Direct

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HRP0086RFC9.7

Chronotype and Type 2 Diabetes Risk in Preadolescents
Direct

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HRP0086RFC9.8

Micro RNA and Diabetic Nephropathy
Direct

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HRP0086RFC10.1

Paternal Loss-of-Function Mutations of GNAS and Growth Retardation in a Mice Model: A Specific Placental Transcriptomic Signature?
Direct

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HRP0086RFC10.2

Dysregulation of Placental Mirna in Maternal Obesity is Associated with Pre-and Post-Natal Growth
Direct

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HRP0086RFC10.3

Vitamin D Depletion in Pregnancy Decreases Survival Time, Oxygen Saturation, Lung Weight and Body Weight in Preterm Rat Offspring
Direct

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HRP0086RFC10.4

Pharmacokinetics of Intravenous Glucagon in Children with Hyperinsulinaemic Hypoglycaemia
Direct

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HRP0086RFC10.5

Phenotype, Genotype and Short term Outcome in Congenital Hyperinsulinism (CHI)
Direct

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HRP0086RFC10.6

Increased Islet Cell Neogenesis and Endocrine Cell Differentiation in Congenital Hyperinsulinism in Infancy
Direct

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HRP0086RFC10.7

Expression of Insulin Receptor Isoforms and Type 1 Insulin-Like Growth Factor Receptor in the Placenta as a Function of Fetal Weight
Direct

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HRP0086RFC10.8

Gestational Diabetes is Associated with Changes in Placental Microbiota and Microbiome
Direct

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HRP0086RFC11.1

Central Hypothyroidism and Biallelic Defect Near the D/ERY Motif of the TRHR Gene
Direct

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HRP0086RFC11.2

The Incidence and Genetic Analysis of Congenital Hypothyroidism in Guangxi, China and the Predictors for Differentiating Permanent and Transient Congenital Hypothyroidism
Direct

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HRP0086RFC11.3

Germline and Somatic DICER1 Mutations in Familial Papillary Thyroid Carcinoma and Multinodular Goiter
Direct

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HRP0086RFC11.4

Thyroid Function in Monozygotic Twins with Intra-Twin Birth-Weight-Differences
Direct

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HRP0086RFC11.5

Novel Homozygous Mutation in the Sodium/Iodide Symporter (NIS) Gene Highlight by Next Generation Sequencing (NGS) in a Patient with Congenital Hypothyroidism
Direct

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HRP0086RFC11.6

Falsely TSH and Free Thyroid Hormone Measurements in Pediatric Patients Treated with High Dose of Biotin
Direct

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HRP0086RFC11.7

Secondary Thyroid Cancer among Childhood Cancer Survivors: A Single Institution Experience
Direct

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HRP0086RFC12.1

Molecular Genetic Diagnosis of Idiopathic Hypogonadotropic Hypogonadism by Using Targeted Next-Generation Sequencing
Direct

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HRP0086RFC12.2

A Novel Mutation of KISS1R Causing a Normosmic Isolated Hypogonadotropic Hypogonadism
Direct

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HRP0086RFC12.3

Next Generation Sequencing and Precocious Puberty: A New Diagnostic Challenge to Identify the Molecular Basis of Complex Diseases
Direct

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HRP0086RFC12.4

Molecular Screening of MKRN3, DLK1 and KCNK9 Genes in Central Precocious Puberty
Direct

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HRP0086RFC12.5

A Novel MKRN3 Nonsense Mutation Causing Familial Central Precocious Puberty
Direct

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HRP0086RFC12.6

Serum Antimullerian Hormone and Inhibin B as Potential Markers for Progressive Central Precocious Puberty in Girls
Direct

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HRP0086RFC12.7

Prevalence of Organic Lesions in Males with Central Precocious Puberty
Direct

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HRP0086RFC12.8

Circulating MKRN3 Levels Decline During Puberty in Healthy Boys
Direct

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HRP0086RFC13.1

Inhibition of Teneurin-2 (TENM2) Leads to Upregulation of UCP1 in Human White Adipocytes
Direct

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HRP0086RFC13.2

The Use of Proteomics in the Assessment of Health Status of Offspring Born after Intracytoplasmic Sperm Injection (ICSI)
Direct

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HRP0086RFC13.3

Effects of Eating Rate on Satiety Hormones, Meal Enjoyment and Memory for Recent Eating: An fMRI Study
Direct

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HRP0086RFC13.4

Which Amount of BMI-SDS Reduction is Necessary to Improve Cardiovascular Risk Factors in Overweight and Obese Children?
Direct

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HRP0086RFC13.5

Protective Potential of Metformin on Membrane Linked Functions in Diabetic Aging Female Rats
Direct

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HRP0086RFC13.6

Laparoscopic Sleeve Gastrectomy in Obese Adolescent Population
Direct

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HRP0086RFC13.7

Early Onset Obesity and Hyperphagia Associated with Defects in the GNAS Gene
Direct

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HRP0086RFC13.8

Measuring Subcutaneous Adipose Tissue Using Ultrasound in Children
Direct

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HRP0086RFC14.1

Important Contribution of GH, GHRHR and GHSR Mutations in Isolated Growth Hormone Deficiency with a Normal Location of the Posterior Pituitary -Functional Characterization of New Variants
Direct

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HRP0086RFC14.2

Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern
Direct

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HRP0086RFC14.3

Whole Exome Sequencing Identifies a GH1 Gene Mutation Causing Familial Isolated Growth Hormone Deficiency with Normal Peak Growth Hormone Concentrations
Direct

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HRP0086RFC14.4

Genetic Diagnosis of Congenital Growth Hormone Deficiency by Massive Parallel Sequencing Using a Target Gene Panel
Direct

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HRP0086RFC14.5

Gene Expression Profiling of Children with GH Deficiency (GHD) Prior to Treatment with Recombinant Human Growth Hormone (r-hGH) is Associated with Growth Response Over Five Years of Therapy
Direct

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HRP0086RFC14.6

Effect of Small Size at Birth, Adult Body Size and Growth Hormone Treatment on Telomere Length
Direct

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HRP0086RFC14.7

GH Influences Plasma Fasting Adropin Concentration in Patients with Turner Syndrome
Direct

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HRP0086RFC14.8

ACAN Mutations in Short Children Born SGA; Growth Response During GH Treatment with Additional GnRHa, and a Proposed Clinical Scoring System
Direct

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HRP0086RFC15.1

A Novel Homozygous Mutation in the Domain AF-2 of Alpha Estrogen Receptor Gene (ESR1), Generating a Bio-Inactive ER[alpha] Mutant, Resulting in Estrogen Resistance with Complex Metabolic Phenotype
Direct

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HRP0086RFC15.2

NR0B1 Frameshift Mutation in a Boy with Precocious Puberty and Normal Adrenal Function
Direct

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HRP0086RFC15.4

The Effect of Sfrp5, Wnt5a, Adiponectin, and Chemerin on Blood Pressure Regulation in Obese Children
Direct

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HRP0086RFC15.5

Effect of Melatonin on Proliferation and Differentiation of Human Dental Pulp Cells
Direct

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HRP0086RFC15.6

Safety of GH in Paediatrics: The GeNeSIS Prospective Observational Study Experience between 1999 and 2015 (NCT01088412)
Direct

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HRP0086RFC15.7

Long-Term Safety and Effectiveness of Daily and Weekly Growth Hormone Treatment in Pediatric GHD Patients (4-Years' Results)
Direct

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HRP0086RFC15.8

Replacement of Male Mini-Puberty
Direct

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HRP0086P1-P1

Leptin is Associated with Serum Aldosterone in Paediatric Subjects, Independently of Body Mass Index, Blood Pressure and Plasma Renin Activity
Direct

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HRP0086P1-P2

Mast Cells and Steroidogenesis in the Human Fetal Adrenal
Direct

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HRP0086P1-P3

Gender-Specific Differences in Hypothalamus-Pituitary-Adrenal Axis Activity in Children: A Meta-Analysis
Direct

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HRP0086P1-P4

Prepubertal Children Born Large for Gestational Age have Lower Serum DHEAS Concentrations than those with Lower Birth Weight
Direct

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HRP0086P1-P5

Whole Exome Sequencing in Patients with Primary Generalized Glucocorticoid Resistance, who did not have Mutations in the NR3C1 Gene
Direct

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HRP0086P1-P6

Novel CYP11A1 Mutations in 15 Patients (13 Families) with Variable Clinical Presentations
Direct

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HRP0086P1-P7

Transient Generalized Glucocorticoid Hypersensitivity Syndrome
Direct

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HRP0086P1-P8

The Effect of Obesity on the Stress Response: The Paradigm of Surgical Stress
Direct

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HRP0086P1-P9

Long-term Anthropometric Outcome of Girls with Non-classical Congenital Adrenal Hyperplasia Diagnosed in Childhood
Direct

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HRP0086P1-P10

Current Dilution Methods Cause Large Variations and Inaccuracies when Making up 1 μg Synacthen Dose
Direct

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HRP0086P1-P11

Evaluation of the Glucocorticoid, Mineralocorticoid, and Adrenal Androgen Secretion Dynamics in A Large Cohort of Patients Aged 6-18 Years with Transfusion-dependent [beta]-Thalassemia Major, with an Emphasis on the Impact of Cardiac Iron Load
Direct

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HRP0086P1-P12

Testicular Adrenal Rest Tumours in 50 Boys, Adolescents and Adult Male with Congenital Adrenal Hyperplasia
Direct

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HRP0086P1-P13

Establishment of Clinical and Lab Algorithms for the Identification Carriers of Mutations in CYP21A2 - A Study of 768 Children and Adolescents
Direct

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HRP0086P1-P14

A Unique Case of Dual Opposing Pathologies
Direct

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HRP0086P1-P15

Individualized Optimization with 17OHP-Saliva Profiles Leads to Changes in Hydrocortisone Dosing Pattern in Children with Congenital Adrenal Hyperplasia
Direct

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HRP0086P1-P16

Cortisol Response to ACTH Stimulation Test in Non-Classical Congenital Adrenal Hyperplasia
Direct

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HRP0086P1-P17

Altered Stress System Activity in Children with ADHD
Direct

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HRP0086P1-P18

Adult Individuals with Classic Congenital Adrenal Hyperplasia Exhibit Deficits in Executive Functions
Direct

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HRP0086P1-P19

Heterozygous Mutations in CYP11A1 Gene can Cause Life-Threatening Salt Wasting and Failure to Thrive
Direct

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HRP0086P1-P20

HIV Drugs as a Possible Cause for Transient 21-Hydroxylase Deficiency in a Preterm Infant
Direct

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HRP0086P1-P21

Increased Salivary and Hair Cortisol and Decreased Salivary Alpha-Amylase Concentrations in Obese Prepubertal Girls
Direct

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HRP0086P1-P22

An Assessment of the Hypothalamic-Pituitary-Adrenal Axis in Children with Prader-Willi Syndrome
Direct

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HRP0086P1-P23

The Urinary Steroidome of Children with Classic 21-Hydroxylase Deficiency Treated with Hydrocortisone
Direct

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HRP0086P1-P24

Adrenal Insufficiency in ROHHADNET Syndrome (Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation and Neural Tumor)
Direct

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HRP0086P1-P25

The Psychosocial Impact of Adrenal Insufficiency and Congenital Adrenal Hyperplasia on Children and their Parents
Direct

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HRP0086P1-P26

Sex-Specific Differences in Hypothalamus-Pituitary-Adrenal Axis Activity in Newborns with Very Low Birth Weight
Direct

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HRP0086P1-P27

Beckwith-Wiedemann Syndrome and Bilateral Phaeochromocytoma: A Diagnostic Challenge
Direct

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HRP0086P1-P28

Combined Glucocorticoid and Mineralocorticoid Deficiency Related to a New NNT Mutation: A Case Report
Direct

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HRP0086P1-P29

Testicular Adrenal Rest Tumours in Patient with X-Linked Adrenoleukodystrophy
Direct

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HRP0086P1-P30

Reference Intervals for the Steroid Hormones of 6 to 14 year Old Normal Male Children with LC-MS Method
Direct

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HRP0086P1-P31

Growth of Children with Congenital Adrenal Hyperplasia (CAH) During the First 2 years of Life - Data from the Duth Longitudinal Registry
Direct

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HRP0086P1-P32

Molecular Confirmatory Test Improves the Accuracy of Congenital Adrenal Hyperplasia Diagnosis in Newborn Screening Program
Direct

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HRP0086P1-P33

Usefulness of Corticotropin Test in Children and Adolescents with Clinical Hyperandrogenism
Direct

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HRP0086P1-P34

Primary Adrenal Insufficiency in Children: Results from a Large Nationwide Cohort
Direct

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HRP0086P1-P35

Follow-up of Growth and Puberty in Girls and Boys with Premature Adrenarche
Direct

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HRP0086P1-P36

Early Onset Hypertension with Primary Hyperaldosteronism through Mutation in the Calcium Channel CACNA1H - Case Report
Direct

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HRP0086P1-P37

DNA Methylation Signatures Associated with Prenatal Dexamethasone Treatment
Direct

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HRP0086P1-P38

Twenty Years Experience in Congenital Adrenal Hyperplasia: Clinical, Hormonal and Molecular Characteristics in a Large Cohort
Direct

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HRP0086P1-P39

Chronic Adrenal Insufficiency Due to a Mutation of Nicotinamide Nucleotide Transhydrogenase 1 (NNT1): Case Report
Direct

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HRP0086P1-P40

Cognitive Functions in Congenital Adrenal Hyperplasia
Direct

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HRP0086P1-P41

RET and TP53 Concomitant Mutations: A Challenging Approach to a Unique Association of High Tumor Predisposing Conditions
Direct

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HRP0086P1-P42

Acute Lysis of a Giant Pediatric Adrenal Cortical Carcinoma Following One Dose of op'DDD
Direct

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HRP0086P1-P43

Severe Hypertension in a Girl: Cushing Syndrome or Apparent Mineralocorticoid Excess Syndrome? Utility of Molecular Study
Direct

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HRP0086P1-P44

An Infant with X-linked Adrenal Hypoplasia Congenita and Xp21 Contiguous Gene Deletion Syndrome
Direct

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HRP0086P1-P45

Polymorphisms Analyze in Gene CYP21A2 Gene Associated with Congenital Adrenal Hyperplasia
Direct

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HRP0086P1-P46

The Effect of Intrauterine Stress on Leukocyte Telomere Length in Newborns
Direct

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HRP0086P1-P47

Predictive Factors for Premature Pubarche in a Large Cohort of Italian Children
Direct

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HRP0086P1-P48

Cardiac Function in Pediatric Patients with Congenital Adrenal Hyperplasia
Direct

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HRP0086P2-P49

Evaluation of the Combination of Anti-androgen and Anti-estrogen Treatment in Classical Congenital Adrenal Hyperplasia in Boys: Retrospective Study of 11 Cases
Direct

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HRP0086P2-P50

Ovarian Cysts in a 46,XX Patient with Congenital Lipoid Adrenal Hyperplasia and with Spontaneous Puberty
Direct

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HRP0086P2-P51

Bone Health Index in Children and Adolescents with Congenital Adrenal Hyperplasia
Direct

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HRP0086P2-P52

Occasional Detection of an Adrenal Incidentaloma in a Female Adolescent Evaluated for Cardiac Arrhythmias
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HRP0086P2-P53

Final Height in Congenital Adrenal Hyperplasia: A Retrospective Study
Direct

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HRP0086P2-P54

Hyperandrogenism in a 12-year Old Girl with a Congenital Porto-Systemic Shunt and Congenital Hepatic Fibrosis
Direct

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HRP0086P2-P55

The Treatment of a Functional Adrenocortical Cancer with Mitotane
Direct

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HRP0086P2-P56

The Effect of Anti-TNF on the Metabolism of Adrenal Hormones; A Steroid Metabolomic Approach
Direct

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HRP0086P2-P57

False-Positive Increases of Steroid Hormone Precursors Mimicking 11[beta]-Hydroxylase-Deficiency in a Preterm Infant
Direct

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HRP0086P2-P58

Isthmic Spondylolisthesis in a Pre-pubertal Boy with Congenital Adrenal Hyperplasia During Aromatase Inhibitor Treatment
Direct

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HRP0086P2-P59

Hospitalisation in Children with Adrenal Insufficiency and Hypopituitarism: Is there a Differential Burden Between Boys and Girls and Between Age Groups?
Direct

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HRP0086P2-P60

A Case of Cushing's Syndrome Due to Adrenocortical Adenoma with Pubarche and Obesity
Direct

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HRP0086P2-P61

Severe Neonatal Cushing Syndrome with Multi-Organ McCune Albright Manifestations
Direct

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HRP0086P2-P62

Final Height Data in a Cohort of Patients with Congenital Adrenal Hyperplasia Treated with Tailored Doses of Hydrocortisone
Direct

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HRP0086P2-P63

The Evolution of Bone Age in Girls with Premature Adrenarche
Direct

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HRP0086P2-P64

Cushing Syndrome Due to Adrenal Adenoma in an Adolescent Patient and Successful Treatment with Laparoscopic Surgery
Direct

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HRP0086P2-P65

A Novel Mutation of DAX-1 (NR0B1) in a Boy with X-linked Adrenal Hypoplasia Congenita
Direct

Abstract PDF
HRP0086P2-P66

Clinical-Laboratory Findings of the Cases with Premature Pubarche and the Value of Acth Stimulation Test in the Differential Siagnosis
Direct

Abstract PDF
HRP0086P2-P67

Successful Medical Management of Severe Neonatal Cushing Syndrome with Metyrapone, Guided by Mass Spectrometry Monitoring
Direct

Abstract PDF
HRP0086P2-P68

Family Character Isolated Pheochromocytoma by Mutation in Vhl gen
Direct

Abstract PDF
HRP0086P2-P69

Exaggerated Adrenarche and Exogenous Obesity: A Diagnostic Challenge
Direct

Abstract PDF
HRP0086P2-P70

Vitamin D Insufficiency is Related to Premature Adrenarche
Direct

Abstract PDF
HRP0086P2-P71

A Case of 17-Years-Old Boy with Relapsing Cushing Disease Presenting Vertebral Compression Fracture
Direct

Abstract PDF
HRP0086P2-P72

The ımpact of 21 Hydroxylase Deficiency on Cardiac Repolarization Changes in Children with 21-hydroxylase-deficient Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P73

Patients with Congenital Adrenal Hyperplasia have Significantly Higher Healthcare Utilisation than the General Paediatric Population
Direct

Abstract PDF
HRP0086P2-P74

Cholestasis and Hypercalcemia Secondary to Panhypopituitarism in a Newborn
Direct

Abstract PDF
HRP0086P2-P75

Clinical Management in Secondary Pseudohypoaldosteronısm: A Case Series
Direct

Abstract PDF
HRP0086P2-P77

Management Dilemmas in a Genetically Female Child with Congenital Adrenal Hyperplasia Raised as a Male
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Abstract PDF
HRP0086P2-P78

Primary Pigmented Nodular Adrenocortical Disease (PPNAD) Justifying a Pediatric Case of ACTH-independent Cushing Syndrome (CS)
Direct

Abstract PDF
HRP0086P2-P79

Three Chinese Patients from Two Kindreds with Aldosterone Synthase Deficiency: Clinical Characteristic with Mutation Analysis Report
Direct

Abstract PDF
HRP0086P2-P80

Addisonian Crisis Due to Autoimmune Adrenalitis in a 14 Year Old Boy with a History of Stem cell Transplantation (HSCT)
Direct

Abstract PDF
HRP0086P2-P81

Assessment of Cardiac Function in Children Followed up for Congenital Adrenal Hyperplasia: A Case Control Study in Cameroon
Direct

Abstract PDF
HRP0086P2-P82

A Novel Mutation of HSD3beta2 Presenting as Hypospadias with Salt-wasting in a Male Infant
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Abstract PDF
HRP0086P2-P83

Testicular Adrenal Rest Tumors in two Young Patients with Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P84

Hyperreninemic Hypoaldosteronism: Clinical and Genetic Features in Pediatric Patients
Direct

Abstract PDF
HRP0086P2-P85

Peculiarities of Manifestation and Short-term Effects of Hormonotherapy in Children With Congenital Adrenal Cortical Hyperplasia
Direct

Abstract PDF
HRP0086P2-P86

Congenital Adrenal Hyperplasia Revealed by Adrenal Nodules
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Abstract PDF
HRP0086P2-P87

Urosepsis or Pseudohypoaldosteronism in a Neonate?
Direct

Abstract PDF
HRP0086P2-P88

A Case Report of Adrenocortical Adenoma in a Young Girl
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Abstract PDF
HRP0086P2-P90

A Genetic Diagnosis of Familial Glucocorticoid Deficiency Resulting in Cessation of Long-term Mineralocorticoid Treatment in Three Siblings
Direct

Abstract PDF
HRP0086P2-P91

Corticosteroid-Induced Adrenal Insufficiency in a Child with T Cell Lymphoblastic Lymphoma
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Abstract PDF
HRP0086P2-P92

A Rare Endocrine Association of Dilated Cardiomyopathy with Congenital Adrenal Hyperplasia due to 11 Beta Hydroxylase Deficiency
Direct

Abstract PDF
HRP0086P2-P93

Use of an F-DEX Monocyte Binding Assay to Measure Steroid Responsiveness of Patients and their Related Donors Undergoing Stem Cell Transplant
Direct

Abstract PDF
HRP0086P2-P94

11[beta]- Hydroxylase Deficiency due to a Novel Compound Heterozygous Mutation and Literature Review
Direct

Abstract PDF
HRP0086P2-P95

Early Adrenarche: A Common Query but not Easily Resolved
Direct

Abstract PDF
HRP0086P2-P96

Assessment of Clinical Effectiveness and Safety of Using Flutamide in Children with Pre-menarche Hierperandrogenismo
Direct

Abstract PDF
HRP0086P2-P97

Congenital Adrenal Hyperplasia - Subtle Presentations with Critical Electrolyte Imbalances and Cardiac Arrhythmias. Experiences from one Hospital
Direct

Abstract PDF
HRP0086P1-P98

Knock in of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-dependent Protein Kinase A Activation: A Model of Acrodysostosis Type 1?
Direct

Abstract PDF
HRP0086P1-P99

Automated Greulich-Pyle Bone Age Determinations in Children with Chronic Endocrine Diseases
Direct

Abstract PDF
HRP0086P1-P100

Cord 25-Hydroxyvitamin D and Infant Cranial Growth: An Odense Child Cohort Study
Direct

Abstract PDF
HRP0086P1-P101

Effect of Bisphosphonates on Bone Fragility Due to Chronic Liver Disease in Ten Children
Direct

Abstract PDF
HRP0086P1-P102

Radiologically Confirmed Fractures in a Scottish Nationwide Cohort of Boys with Duchenne Muscular Dystrophy
Direct

Abstract PDF
HRP0086P1-P103

Monostotic Fibrous Dysplasia is a Single Disorder Caused by Somatic Mosaic Activating Mutations in GNAS
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Abstract PDF
HRP0086P1-P104

Clinically Significant Fracture Incidence in Czech Children: A Population-based Study
Direct

Abstract PDF
HRP0086P1-P105

Effects of Selective GPER-1 Agonist G1 on Bone Growth
Direct

Abstract PDF
HRP0086P1-P106

Bone Mineral Density, Pubertal Status and Ability to Walk are Associated to Fracture Incidence in Patients with Rett Syndrome
Direct

Abstract PDF
HRP0086P1-P107

Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome
Direct

Abstract PDF
HRP0086P1-P108

Tolerability and Feasibility of Whole Body Vibration and its Effects on Muscle Function and Bone Health in Patients with Dystrophinopathy
Direct

Abstract PDF
HRP0086P1-P109

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta
Direct

Abstract PDF
HRP0086P1-P110

Increase in Sclerostin After Rapid Weight Loss in Children
Direct

Abstract PDF
HRP0086P1-P111

Impact of Conventional Medical Treatment on Bone Mineral Density and Bone Turnover in Adult XLH Patients: A 6 Year Cohort Study
Direct

Abstract PDF
HRP0086P1-P112

Bone Health and Body Composition in Childhood Onset Growth Hormone Deficiency at Time of Initial Evaluation and Retesting
Direct

Abstract PDF
HRP0086P1-P113

Extension of The Bone Health Index to Adults, and Reference Curves of Four Indices of Cortical Bone for Healthy Europeans
Direct

Abstract PDF
HRP0086P1-P114

Extension of Automated Bone Age Determination to the End of Puberty
Direct

Abstract PDF
HRP0086P1-P115

A European Survey to Identify New Roads for Care, Training and Research Around Rare Metabolic Bone Diseases
Direct

Abstract PDF
HRP0086P1-P116

Clinical and Molecular Characterization of 25-Hydroxylase Deficiency in Saudi Patients
Direct

Abstract PDF
HRP0086P1-P117

No Severe Hypercalcemia During a 12-Month High-Dose Vitamin D Intervention in Infants
Direct

Abstract PDF
HRP0086P1-P118

Management of Tracheobronchomalacia During Asfotase Alfa Treatment in Infants with Perinatal-onset Hypophosphatasia: A Case Series
Direct

Abstract PDF
HRP0086P1-P119

Novel p.Asn628Ser Heterozygous Mutation in FGFR1 is Associated with Hartsfield Syndrome and Tumoral Calcinosis
Direct

Abstract PDF
HRP0086P1-P120

Practicalities of Bisphosphonate use in UK Paediatric Tertiary Centres
Direct

Abstract PDF
HRP0086P1-P121

Computer-assisted Diagnosis of Dyschondrosteosis Based on Skeletal X-ray Geometry
Direct

Abstract PDF
HRP0086P1-P122

Bisphosphonates Therapy in Girls with Rett Syndrome and Bone Fragility
Direct

Abstract PDF
HRP0086P1-P123

Skeletal Manifestations in APECED
Direct

Abstract PDF
HRP0086P1-P124

Two French Families with Vitamin D Dependency Rickets Type 1B Harbor Homozygous Recessive Expression Of CYP2R1 Mutations L99P and G42_L46DEL INSR
Direct

Abstract PDF
HRP0086P1-P125

Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children
Direct

Abstract PDF
HRP0086P1-P126

Impact of Intercurrent Illness on Calcium Homeostasis and Hypoparathyroidism Management
Direct

Abstract PDF
HRP0086P1-P127

Transient Pseudohypoaldosteronism and Failiure to Thrive in A 5-Month-Old Infant
Direct

Abstract PDF
HRP0086P1-P128

Childhood Cancer Survivors (CCS) are at High Risk of Reduced Bone Mass During the Second Decade of Life
Direct

Abstract PDF
HRP0086P1-P129

Trabecular Bone Score in Children from Mexico City: Preliminary Report
Direct

Abstract PDF
HRP0086P1-P130

Triple X Syndrome: An Evaluation of Bone Mineral Status and Metabolism
Direct

Abstract PDF
HRP0086P1-P131

Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes
Direct

Abstract PDF
HRP0086P1-P132

Spinal and Forearm Bone Mineralization in Adolescents with Klinefelter Syndrome
Direct

Abstract PDF
HRP0086P1-P133

Treatment with Zoledronic Acid in Children with Duchenne Muscular Dystrophy
Direct

Abstract PDF
HRP0086P1-P134

A RCT Comparing the Effect of Three Different Vitamin D Supplementation Regimens on Se 25 OH Vit D in Asymptomatic Vit D Deficient Children
Direct

Abstract PDF
HRP0086P1-P135

Low Bone Mineral Density in Adolescents with Leukemia After Hematopoietic Stem Cell Transplantation
Direct

Abstract PDF
HRP0086P1-P136

Growth Characteristics of a Girl with Multicentric Carpo-Tarsal Osteolysis Caused by Novel Mutation in the MAFB Gene
Direct

Abstract PDF
HRP0086P1-P137

Treatment Experience and Long-Term Follow-Up Data in Two Severe Neonatal Hyperparathyroidism Cases
Direct

Abstract PDF
HRP0086P1-P138

Biochemical Parameters Associated with Serum Intact FGF23 Levels in Patients with X-Linked Hypophosphatemic Rickets
Direct

Abstract PDF
HRP0086P1-P139

Dental Effects of Intravenous Bisphosphonate When Administered in Early Infancy
Direct

Abstract PDF
HRP0086P1-P140

Bone Mass and Vitamin D Status in Children and Adolescents with Generalized Epidermolysis Bullosa
Direct

Abstract PDF
HRP0086P1-P141

Off-Label Use of the Aromatase Inhibitor Letrozole in Pubertal Boys to Improve Final Height: Laboratory, Auxological and Bone Age Data
Direct

Abstract PDF
HRP0086P1-P142

Effect of Bisphosphonates and Denosumab on Trabecular Bone: Results of a Pilot Study in Children with Osteogenesis Imperfecta
Direct

Abstract PDF
HRP0086P1-P143

Impact of Anti-Tumour Necrosis Factor Therapy on the Insulin Like Growth Factor Axis and Bone Development in Childhood Crohn's Disease
Direct

Abstract PDF
HRP0086P1-P144

Effects of Phylloquinone and Magnesium on ATDC5 Prechondrocytes
Direct

Abstract PDF
HRP0086P1-P145

To Study the Efficacy and Safety of Growth Hormone (GH) Therapy in Children with Pycnodysostosis
Direct

Abstract PDF
HRP0086P2-P146

Bone Mineral Status and Metabolism in Patients with Williams-Beuren Syndrome
Direct

Abstract PDF
HRP0086P2-P147

The Beneficial Effect of Cinacalcet on the Treatment of vitD Resistant Rickets
Direct

Abstract PDF
HRP0086P2-P148

A Preliminary Report on Body Composition Profile of Young Patients with Chronic Hemolytic Conditions
Direct

Abstract PDF
HRP0086P2-P149

Bone Status in a Patient with IGF-I Receptor Deletion Syndrome: Bone Quality and Structure Evaluation Using DXA, pQCT, and QUS
Direct

Abstract PDF
HRP0086P2-P150

Prevalence of Vitamin D Deficiency in Haitian Infants and Children
Direct

Abstract PDF
HRP0086P2-P151

Progressive Development of PTH Resistance in Patients with Maternal GNAS Inactivating Mutations
Direct

Abstract PDF
HRP0086P2-P152

Effect of Hydroxyurea Therapy on Growth Parameters in Older Children with Sickle Cell Disease
Direct

Abstract PDF
HRP0086P2-P153

Evaluation of ALP Value in Early Prediction of the Effects of Growth Hormone Treatment in Children with Growth Hormone Deficiency (GHD)
Direct

Abstract PDF
HRP0086P2-P154

Comparison of Two Different Stoss Therapy Doses in Children with Vitamin D Deficiency or Insufficiency without Rickets
Direct

Abstract PDF
HRP0086P2-P155

Bisphosphonate Treatment of Hypercalcemia in a Child with Jansen'S Metaphyseal Chondrodysplasia
Direct

Abstract PDF
HRP0086P2-P156

Physical Exercise Level is Associated to Peak Bone Mass in Undergraduate Students
Direct

Abstract PDF
HRP0086P2-P157

A Case with Lethal Perinatal Hypophosphatasia
Direct

Abstract PDF
HRP0086P2-P158

Anthropometric and Nutritional Parameters in Egyptian Children with Osteogenesis Imperfecta: Effect of Zoledronic Acid Therapy
Direct

Abstract PDF
HRP0086P2-P159

Low Bone Mineral Density in Adolescents with Joint Hypermobility
Direct

Abstract PDF
HRP0086P2-P160

Fractures in Children with Type 1 Diabetes are Associated with Poorer Bone Mineral Status and Glycaemic Control
Direct

Abstract PDF
HRP0086P2-P161

Identification of Predictor Factors of Growth Outcome in Children with Hypophosphatemic Rickets
Direct

Abstract PDF
HRP0086P2-P162

Effects of Socioeconomic Status on Bone Mineral Density and Vitamin D Concentrations in Healthy Female College Students
Direct

Abstract PDF
HRP0086P2-P163

Bone Health Index is Low at Diagnosis of Growth Hormone Deficiency, and Improves During Growth Hormone Therapy
Direct

Abstract PDF
HRP0086P2-P164

Vitamin D Dependent Rickets Type II in Saudi Children
Direct

Abstract PDF
HRP0086P2-P165

Bone Health and Metabolic Syndrome in Childhood Cancer Survivors
Direct

Abstract PDF
HRP0086P2-P166

Diversity in Phenotype of Two Siblings and their with X-Linked Hypophosphatemic Rickets due to PHEX Mutation
Direct

Abstract PDF
HRP0086P2-P167

Expression of Brdu, VEGF, IGF-1R and Change of the Growth Plates from Sex Hormone-Inhibited Adolescents Rats - Pilot Study
Direct

Abstract PDF
HRP0086P2-P168

A Case of Genetically Proven Carbonic Anhydrase II Deficiency
Direct

Abstract PDF
HRP0086P2-P169

Rickets as Precocious Sign of Celiac Disease
Direct

Abstract PDF
HRP0086P2-P170

Clinical and Genetic Analysis of Five Patients with Vitamin D-Dependent Rickets Type 1A
Direct

Abstract PDF
HRP0086P2-P171

About a Case of a Family of Pycnodysostose
Direct

Abstract PDF
HRP0086P2-P172

Potential Role of Vitamin D in Pathogenesis of Acute Rheumatic Fever
Direct

Abstract PDF
HRP0086P2-P173

Bartter Syndrome with Bone-Destroying Hyperparathyroidism: About Two Cases, Genetically Proved, with Long-Lasting Follow-Up
Direct

Abstract PDF
HRP0086P2-P174

Management of Hypoparathyroidism: Follow-Up of 20 Patients
Direct

Abstract PDF
HRP0086P2-P175

Assessing the Serum Levels of Ferritin and Selenium in Three Important Infections of Childhood, Compared to a Control Group
Direct

Abstract PDF
HRP0086P2-P176

A Case: Hydrocephalus Secondary to Suprasellar Arachnoid Cyst with Reset Osmostat and Isolated GH Deficiency
Direct

Abstract PDF
HRP0086P2-P177

Cinacalcet Treatment in a Child with Concurrent Juvenile Idiopathic Arthritis and Hypocalciuric Hypercalcemia
Direct

Abstract PDF
HRP0086P2-P178

Pseudohypoparathyroidism 1a with Turner's Syndrome: A Diagnostic Dilemma
Direct

Abstract PDF
HRP0086P2-P179

Bisphosphonate Use for Control of Chronic Severe Bone Pain in Children with Malignancy Associated Bone Involvement
Direct

Abstract PDF
HRP0086P2-P180

Renal Tubular Acidosis Causing Severe Growth Delay and Rickets in Two Siblings in Haiti
Direct

Abstract PDF
HRP0086P2-P181

Pseudohypoparathyroidism Type IB Associated to Assisted Reproductive Technologies: Case Report
Direct

Abstract PDF
HRP0086P2-P182

Primary Hyperparathyroidism- A Cause of Metabolic Syndrome in Children?
Direct

Abstract PDF
HRP0086P2-P183

Hyperphosphatemic Familial Tumoral Calcinosis: Novel Indication to Sevelamer Carbonate
Direct

Abstract PDF
HRP0086P2-P184

DiGeorge Syndrome and 10p Deletion
Direct

Abstract PDF
HRP0086P2-P185

Multifocal Osteonecrosis after Short Term Methylprednysolon Therapy: A Case Report
Direct

Abstract PDF
HRP0086P2-P186

Unclear Origin of Avascular Necrosis - Clinical Case
Direct

Abstract PDF
HRP0086P2-P187

Is NOTCH-Sonic Hedgehog Signalling Pathway the Missing Link Between Hajdu-Cheney Syndrome and Syringomyelia?
Direct

Abstract PDF
HRP0086P2-P188

The Unexpected Cause of Vitamin D Deficiency in a Resource Limited Setting: A Rare Case Report of Primary Intestinal Lymphangiectasia
Direct

Abstract PDF
HRP0086P2-P189

About a Case of Dwarfism Idiopathic
Direct

Abstract PDF
HRP0086P1-P190

The Association of HLA Class II, CTLA-4 and PTPN22 Genetic Polymorphisms and [beta]-Cell Autoantibodies in Development of Type I Diabetes in Patients with Autoimmune Thyroid Disease
Direct

Abstract PDF
HRP0086P1-P191

Insulin Pump Does Not Allow a Better Control than Injections in Childhood Type 1 Diabetes (T1d) in the ISIS-Diab Cohort
Direct

Abstract PDF
HRP0086P1-P192

Diagnostic Features of Lipodystrophy in Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P193

Recombinant Human Insulin-Like Growth Factor 1 (rh IGF1) Treatment of a Case of Leprechaunism: A Two and a Half Year Follow-Up
Direct

Abstract PDF
HRP0086P1-P194

Longitudinal Monitoring of Pediatric Insulin Treatment in Germany and Austria: Age-Dependent Analysis of 63 967 Children and Adolescents with Type 1 Diabetes from the DPV Registry
Direct

Abstract PDF
HRP0086P1-P195

Two Patients with HADH (SCHAD) Hyperinsulinism without Detectable 3-Hydroxybutyrylcarnitine/3-Hydroxyglutarate
Direct

Abstract PDF
HRP0086P1-P196

Development of Type 1 Diabetes in a Child with Inherited CD59 Deficiency Treated with Eculizumab
Direct

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HRP0086P1-P197

Diagnosis of Non-Autoimmune Paediatric Diabetes by Targeted Next Generation Sequencing (NGS): Findings in Two Families with Rare Mono- and Digenic forms of Diabetes
Direct

Abstract PDF
HRP0086P1-P198

Neonatal Siabetes, Gallbladder Agenesis and Cholestatic Giant Cell Hepatitis: A Novel Homozygote Mutation in PDX-1 Gene
Direct

Abstract PDF
HRP0086P1-P199

Anthropometry and Glucose Homeostasis in a Patient with Donohue Syndrome (Homozygous Insulin Receptor Mutation): Effect of Continuous s.c. rIGF-I Therapy
Direct

Abstract PDF
HRP0086P1-P200

Driving Paediatric Diabetes Care Forward in the UK: Improvements in Outcomes in the North West Following National Initiatives
Direct

Abstract PDF
HRP0086P1-P201

Non-Surgical Treatment of Diazoxide-Resistant of Early Diffuse Hyperinsulinism Using Long-Acting Octreotide, A Somaatostatin Analog: Follow-Up of Six Cases
Direct

Abstract PDF
HRP0086P1-P202

Screening for Autonomic Neuropathy in Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P203

Diabetes Mellitus Caused by Bone Marrow Transplantation and Total Body Irradiation - Experience from a Regional Single Centre
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Abstract PDF
HRP0086P1-P204

A Syndrome of Permanent Neonatal Diabetes Mellitus and Neurological Abnormalities due to a Novel Homozygous Missense c.449T>A (p.I150N) Mutation in NEUROD1 Gene
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Abstract PDF
HRP0086P1-P205

Are We Screening Appropriate Age Group for Early Diagnosis of Cystic Fibrosis Related Diabetes in UK?
Direct

Abstract PDF
HRP0086P1-P206

When to Screen for Coeliac Disease in Children with Type 1 Diabetes Mellitus: The Controversy
Direct

Abstract PDF
HRP0086P1-P207

Interrelation between ACE Gene I/D Polymorphism and Chronic Kidney Disease Severity in Uzbek Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P208

Improvement of Diabetic Screening System for School Children Achieved by Close Cooperation with a Local Government of Atsugi City
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Abstract PDF
HRP0086P1-P209

Association between Hypothalamus-Pituitary Adrenal Axis Activity and Anxiety in Prepubertal Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P210

Screening for Liver Disease in Children and Adolescents with Type 1 Diabetes Mellitus: A Cross-sectional Analysis
Direct

Abstract PDF
HRP0086P1-P211

Exploration of Social Network, Social Integration, and Socioeconomic Status in Families with Young Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P212

Permanent Neonatal Diabetes Mellitus due to a Novel Homozygous GCK Mutation in a Premature Baby with IUGR and Its Management
Direct

Abstract PDF
HRP0086P1-P213

The Impact of Diet on Insulin Dynamics over a 2-Year Period in Children with a Family History of Obesity
Direct

Abstract PDF
HRP0086P1-P214

Analysis of Short-Term Efficacy of MiniMed 640G with SmartGuard in Pediatric Patients with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P215

The Influence of sz-Cell Autoimmunity on Cystic Fibrosis Related Diabetes Mellitus - A DPV Registry Analysis
Direct

Abstract PDF
HRP0086P1-P216

Thyroid and Islet Autoantibodies Predict Autoimmune Thyroid Disease Already at Diagnosis of Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P217

Hemolysis in a Girl with Type 1 Diabetes Mellitus and Glucose-6-Phosphate Dehydrogenase Deficiency
Direct

Abstract PDF
HRP0086P1-P218

Clinical Characteristics and Molecular Analysis of Patients with Neonatal Diabetes
Direct

Abstract PDF
HRP0086P1-P219

Impact of Continuous Glucose Monitoring System on Therapy of Cystic Fibrosis Related Diabetes in Children and Young Adults
Direct

Abstract PDF
HRP0086P1-P220

Effect of Allopurinol Versus Angiotensin Converting Enzyme Inhibitors in Decreasing Microalbuminuria in Type 1 Diabetic Patients
Direct

Abstract PDF
HRP0086P1-P221

Continuous Glucose Monitoring and Hypoglycemia Unawareness in Children and Adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P222

Transient, Neonatal Hyperinsulinemic Hypoglycemia May be Monogenetic, Not Only Secondary to Fetal Life Events
Direct

Abstract PDF
HRP0086P1-P223

The Relationship between the Serum Irisin Levels and the Metabolic Control in adolescents with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P224

Space-time Environmental Associations in Childhood Type 1 Diabetes (T1D). A Case-control Geographical Approach in the ISIS-Diab Cohort
Direct

Abstract PDF
HRP0086P1-P225

Association Between Vascular Endothelial Markers and Carotid Intima-media Thickness in Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P227

Rising of Type 1 Diabetes Mellitus Incidence in Chilean Children Between 2006 and 2014
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Abstract PDF
HRP0086P1-P228

Frequency and Risk Factors of Depression in Type 1 Diabetes in a Developing Country
Direct

Abstract PDF
HRP0086P1-P229

Phenotypic Variability of Identical Mutations in the ABCC8 Gene in Two Families
Direct

Abstract PDF
HRP0086P1-P230

Growth and Glucose Metabolism after Allogenic Bone Marrow Transplantation for Thalassemia Major
Direct

Abstract PDF
HRP0086P1-P231

A Rare Form of Insulin Resistance with Pseudoacromegaly
Direct

Abstract PDF
HRP0086P1-P232

Extrahepatic Biliary Atresia in Combination with Toxic Cholestasis Due to Glibenclamide in a Case of Neonatal Diabetes
Direct

Abstract PDF
HRP0086P1-P233

Higher-Than-Conventional Subcutaneous Regular Insulin Doses Following Diabetic Ketoacidosis are Associated with Better Short-term Glycemic Control
Direct

Abstract PDF
HRP0086P1-P234

Assessment of Selected Carbohydrate Parameters in Children Exposed to Gestational Diabetes in utero
Direct

Abstract PDF
HRP0086P1-P235

The Genetic Causes and Phenotypic Characteristics of Egyptian Patients with Neonatal Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P236

Does Adherence to a High HbA1c Policy Improve Outcomes in a Paediatric Diabetic Clinic Population?
Direct

Abstract PDF
HRP0086P1-P237

The Prevalence of Diabetic Ketoacidosis in Children with New-Onset Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P238

Correction of Carnitine Deficiency in Children with Recent Onset Type 1 Diabetes
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Abstract PDF
HRP0086P1-P239

Fetal Growth Restriction Due to Maternal Congenital Hyperinsulinism Associated with a Novel Variant in GLUD1 and Intrauterine Diazoxide Exposure
Direct

Abstract PDF
HRP0086P1-P240

Effect of Vitamin D Supplementation on Lipid Profile in Vitamin D Deficient T1D Patients with Dyslipidemia
Direct

Abstract PDF
HRP0086P1-P241

Renal Functional Reserve in Children with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P1-P242

The Prognostic Role of Non-alcoholic Fatty Liver Disease in Children with Type 1 Diabetes Mellitus with and without Dyslipidemias
Direct

Abstract PDF
HRP0086P1-P243

Associated and Familial Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus
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Abstract PDF
HRP0086P1-P244

Factors Affecting Dyslipidaemia in Children and Young People with Type 1 Diabetes Mellitus: A Multicentre Study
Direct

Abstract PDF
HRP0086P1-P246

Wolcott Rallison Syndrome due to a Novel Mutation in EIF2AK3 Gene
Direct

Abstract PDF
HRP0086P1-P247

Which is the Best Site for Catheter Placement in Young Children with Type 1 Diabetes (T1D) and CSII?
Direct

Abstract PDF
HRP0086P1-P248

GCK Mutations in Chinese MODY2 Patients: A Family Pedigree Report and Review of Chinese Literature
Direct

Abstract PDF
HRP0086P1-P249

Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P250

Type 1 Diabetes (T1D) Management with Few Blood Glucose (BG) Measurements but Frequent Free Adjustment of Treatment with Cell Phones or E-mails
Direct

Abstract PDF
HRP0086P1-P251

Metabolic Impairments among Adult Survivors of Paediatric Abdominal and Pelvic Tumours in the St Jude Lifetime Cohort Study
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Abstract PDF
HRP0086P1-P252

Clinical Case of a 10-year-old Girl with Papillomatosis Due to Severe Insulin Resistance Type A
Direct

Abstract PDF
HRP0086P1-P253

Sulphonylurea Treatment in a Patient with Intermediate DEND Syndrome
Direct

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HRP0086P1-P254

A Case-Control Search of Environmental (E) Factors for Childhood Type 1 Diabetes (T1D) Using Lifeline Questionnaires in the ISIS-Diab Cohort
Direct

Abstract PDF
HRP0086P1-P255

Transient Neonatal Diabetes Mellitus in Hanoi, Vietnam: Clinical Feature and Outcome
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Abstract PDF
HRP0086P1-P256

The Incidence of Type 1 Diabetes in the Pediatric Population in Pomeranian Region in Poland
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Abstract PDF
HRP0086P1-P257

Health-Related Quality of Life and its Associated Factors in Children With Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P258

Possible Monogenic Diabetes Mellitus Including Mody is Highly Prevalent in Korean Children with Diabetes Mellitus
Direct

Abstract PDF
HRP0086P1-P259

Phenotype and Clinical Course of Diabetes Mellitus in Individuals with Pancreatic Hypoplasia Due to a PTFA Enhancer Mutation
Direct

Abstract PDF
HRP0086P1-P260

Microalbuminuria in Type 1 Diabetes - Audit of Management of Children and Adolescents in a Single Diabetes Centre
Direct

Abstract PDF
HRP0086P1-P261

Johansson-Blizzard Syndrome with Pan-hypopituitrism, Type 2 Diabetes and Pancreatic insufficiency: Effect of Treatment
Direct

Abstract PDF
HRP0086P2-P262

Comparison of the Occurrence of Islet Autoantibodies in Siblings of Patients with Type 1 Diabetes Mellitus to Healthy Children
Direct

Abstract PDF
HRP0086P2-P263

The Role of 24-h Ambulatory Blood Pressure Monitoring in Children and Adolescents with Type 1 Diabetes: Early Experience of a Single Centre
Direct

Abstract PDF
HRP0086P2-P264

Clinical, Biochemical, Genetic and Immunological Features of Mexican Recent-Onset Type 1 Diabetes Patients
Direct

Abstract PDF
HRP0086P2-P265

Efficacy and Safety of Continuous Subcutaneous Insulin Infusion Treatment in Pre-schoolers. Long Term Experience of a Tertiary Care Centre in Spain
Direct

Abstract PDF
HRP0086P2-P266

Gene-Environment (GxE) Interactions in Childhood Type 1 Diabetes (T1D): A Case-only Geographical Approach in the ISIS-Diab Cohort
Direct

Abstract PDF
HRP0086P2-P267

NBAS Mutations, a New Monogenic Cause of DISOPHAL, a New Syndrome with Type 1 Diabetes (T1D)
Direct

Abstract PDF
HRP0086P2-P268

A Patient with a Rare Monogenic Diabetes Syndrome
Direct

Abstract PDF
HRP0086P2-P269

Which Group of Children Achieved the Best Results During Insulin Pump Therapy - Long-term Outcome in Children with Type 1 Diabetes?
Direct

Abstract PDF
HRP0086P2-P270

Seasonality of Type 1 Diabetes in Children and Adolescents According to Date of Diagnosis and Date of Birth in a Large Diabetes Centre
Direct

Abstract PDF
HRP0086P2-P271

Abnormal Glucose Level in Patients with Thalassemia Major
Direct

Abstract PDF
HRP0086P2-P272

A Case Report of Wolfram Syndrome due to a Novel Homozygous Mutation in WFS1 Gene
Direct

Abstract PDF
HRP0086P2-P273

Lower Basal Insulin Dose - Better Control in Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P274

'Comparison of Neutrophil/Lymphocyte Ratio According to Degree of Glycemic Control in Children with Recent-onset Type 1 and Type 2 Diabetes
Direct

Abstract PDF
HRP0086P2-P275

Pancreatic Reserve and Metabolic Control of Type 1 Diabetes in a Cohort of Spanish Children and Adolescent
Direct

Abstract PDF
HRP0086P2-P276

The Best Practice Tariff for Paediatric Diabetes Care within England: A District General Experience
Direct

Abstract PDF
HRP0086P2-P277

Prevalence of Cardiovascular Risk Factors and Obesity in Youth with Type 1 Diabetes in Lithuania
Direct

Abstract PDF
HRP0086P2-P278

Childhood Type 1 Diabetes (T1D) Management with e-learning through Self-educational Tools
Direct

Abstract PDF
HRP0086P2-P279

Mucormycosis and Type 1 Diabetes: A Case Report
Direct

Abstract PDF
HRP0086P2-P280

Insulin Pump Therapy in Type 1 Diabetes: The Indian Experience
Direct

Abstract PDF
HRP0086P2-P281

Child with Mutation in GATA 6 Gene - Case Report
Direct

Abstract PDF
HRP0086P2-P282

A Case Report of a 14 Year Old Female with a Known History of Type 1 Diabetes Mellitus Who Developed Tracheal Stenosis as a Result of Prolonged Intubation from Diabetic Ketoacidosis and Subsequently Developed Acute Pancreatitis
Direct

Abstract PDF
HRP0086P2-P283

Continuous Glucose Monitoring Can Alleviate Parental Fear of Hypoglycaemia in Children with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P284

The Implementation of a System of Continuous Monitoring of Blood Glucose and Open (FREE STYLE FREE) Improves Metabolic Control of Affected Children DMtipo1
Direct

Abstract PDF
HRP0086P2-P285

Permanent Neonatal Diabetes by Gene Mutation KCNJ11. Evolution and Treatment after Three Years with Sulphonylureas
Direct

Abstract PDF
HRP0086P2-P286

Atypical Cystic Fibrosis Adolescent Case Study (with Normal Sweat Test) Referring with Diabetes Mellitus Symptoms Found to Carry Homozygous R352Q Mutation
Direct

Abstract PDF
HRP0086P2-P287

Diabetic Ketoacidosis Risk Factors in the Initial Presentation of Type 1 Diabetes Mellitus in Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P288

Prevalence of Polycystic Ovary Symdrome and its Clinical Profile in Young Females with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P289

The Frequency of Diabetic Ketoacidosis in Children and Adolescents with Newly Diagnosed Type 1 Diabetes Mellitus: A Single Centre Experience in Turkey
Direct

Abstract PDF
HRP0086P2-P290

Wolcott-Rallison Syndrome: Clinical Case Presentation
Direct

Abstract PDF
HRP0086P2-P291

The Story of a de novo Heterozygous HNF1A Mutation
Direct

Abstract PDF
HRP0086P2-P292

Use of Continuous Glucose Monitoring Helps Selecting Insulin Therapy in Thalassemic Adolescents with Glycemic abnormalities
Direct

Abstract PDF
HRP0086P2-P293

Impact of Demographic Factors on Diabetic Ketoacidosis Occurrence at Type 1 Diabetes Onset in Childhood
Direct

Abstract PDF
HRP0086P2-P294

Differences in Hba1c among Different Ethnicities; Is it just a Matter of Mean Glycaemia?
Direct

Abstract PDF
HRP0086P2-P295

Ischemic Intestinal Necrosis as a Rare Complication of Diabetic Ketoacidosis in a Child with New-Onset Type I Diabetes: A Case Report
Direct

Abstract PDF
HRP0086P2-P296

Diabetes - a Rare Complication of Ataxic Telangiectasia Presenting in Childhood
Direct

Abstract PDF
HRP0086P2-P297

Clinical and Demographic Characteristics of Patients with Type 1 Diabetes Mellitus and correlation with risk factors: A South Indian Database
Direct

Abstract PDF
HRP0086P2-P298

Insulin Response at Standard Glucose Load in Children With Normal, Low and Excessive Body Mass
Direct

Abstract PDF
HRP0086P2-P299

Initial Presentation of Subjects with Type 1 Diabetes: A Change in Spectrum
Direct

Abstract PDF
HRP0086P2-P300

Evaluation of the Epidemiological, Presenting and Follow-up Characteristics and their Impacts on the Glycemic Control in a Large Cohort of Pediatric Type 1 Diabetes Mellitus Patients from Southeastern Anatolian Region of Turkey
Direct

Abstract PDF
HRP0086P2-P301

HbA1C and IGF-1 Levels in Diabetic Children Treated with Vitamin D
Direct

Abstract PDF
HRP0086P2-P302

Long-Term Follow-Up of Non-Diabetic Obese Children and Adolescents Treated with Metformin
Direct

Abstract PDF
HRP0086P2-P303

Understanding the Molecular and Genetic Basis of Complex Syndromes of Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P304

Cardiovascular Risk and Long Term Follow-up of Turkish Children with Type 2 Diabetes: Single Center Experience
Direct

Abstract PDF
HRP0086P2-P305

Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine
Direct

Abstract PDF
HRP0086P2-P306

Maturity-Onset Diabetes of the Young (MODY): Tracking and Clinical Follow-up
Direct

Abstract PDF
HRP0086P2-P307

Evaluation of Autoimmune Thyroiditis Development on Onset and During Follow Up in Cases with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P308

The Autoimmune Hypothesis for Acute Bilateral Cataract in Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P309

Clinical Characteristics of Latent Autoimmune Diabetes in Youth (Type 1.5 DM)
Direct

Abstract PDF
HRP0086P2-P310

Diabetic Ketoacidosis: Clinical Features and Precipitating Factors at DEMPU
Direct

Abstract PDF
HRP0086P2-P311

Diabetes Distress in Adolescents and Young Adults with Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P312

A Novel Glucokinase Gen Mutation: Mody Type-2 Case
Direct

Abstract PDF
HRP0086P2-P313

Congenital Hyperinsulinism in a Resource Limited Setting: Overcoming Barriers towards a Survival Path
Direct

Abstract PDF
HRP0086P2-P314

Vitamin D Levels and Relations with Clinical and Laboratory Findings in Children with Newly Diagnosed Type 1 Diabetes
Direct

Abstract PDF
HRP0086P2-P315

Lipid Profile, Lipid Per-Oxidation and Trace Elements Status in Libyan Males with Type II Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P316

Cystic Fibrosis Related Diabetes
Direct

Abstract PDF
HRP0086P2-P317

Type 1 Diabetes in Childhood: An 8-year Experience
Direct

Abstract PDF
HRP0086P2-P318

A Rare Reason of Type 2 Diabetes: Alstrom Syndrome
Direct

Abstract PDF
HRP0086P2-P319

The Relationship among Cardiac T2*, Liver T2* and Abnormal Glucose in Patients with Thalassemia Major
Direct

Abstract PDF
HRP0086P2-P320

Hyperglycaemia in a Boy of 13 years old: Not always Type 1 Diabetes Mellitus. A Case Report
Direct

Abstract PDF
HRP0086P2-P321

Achievement of Metabolic Parameter Goals in Children and Adolescent with Type 1 Diabetes According to the Latest ADA/ISPAD Standards of Medical Care in Diabetes in a Pediatric Diabetes Clinic in North Greece
Direct

Abstract PDF
HRP0086P2-P322

Clinical and Laboratory Characteristics of Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P323

Prevalence of Acute Metabolic Complications in Children with Type I Diabetes Admitted to the Children Hospital in Qazvin, Iran (2005-2014)
Direct

Abstract PDF
HRP0086P2-P324

Glargine versus Detemir Insulin During the Honeymoon Phase in a Child with Type1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P325

Diabetic Ketoacidosis and Multiple Organ Failure Syndrome: A Case Study
Direct

Abstract PDF
HRP0086P2-P326

Neonatal Diabetes Associated with Transaminitis in a Growth Retarded Infant
Direct

Abstract PDF
HRP0086P2-P327

Benefits of Switching Insulin from Twice Daily to Multiple Daily Injections on Glycaemic Control in Children with Type 1 Diabetes Mellitus in Sri Lanka at the Lady Ridgeway Hospital, Sri Lanka
Direct

Abstract PDF
HRP0086P2-P328

Rapid Acting Insulin Analogue Treatment in Children and Adolescents with Type 1 Diabetes Mellitus; Insulin Glulisine Experience
Direct

Abstract PDF
HRP0086P2-P329

The Prevalence of Dyslipidemia and Associated Factors in Children and Adolescent with Type I Diabetes
Direct

Abstract PDF
HRP0086P2-P330

Lipid Metabolism in Children with Diabetes Mellitus Type 1
Direct

Abstract PDF
HRP0086P2-P331

Prevalence of Celiac Disease in Children and Adolescents with Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P332

Evaluating the Impact of the Diagnosis and Management of a Child with Type 1 Diabetes on Parents
Direct

Abstract PDF
HRP0086P2-P333

Association Between Socioeconomic Status and Glycemic Control in Type 1 Diabetes Mellitus
Direct

Abstract PDF
HRP0086P2-P334

Minimally Invasive Surgical Interventions in the Treatment of Primary Persistent Hyperinsulinemic Hypoglycemia of Infancy
Direct

Abstract PDF
HRP0086P1-P335

Complete Androgen Insensitivity Syndrome Caused by a Deep Intronic Pseudoexon-Activating Mutation in the Androgen Receptor Gene
Direct

Abstract PDF
HRP0086P1-P336

Polycystic Ovary Syndrome in Adolescence: New Therapeutic Approach with Inositol and Alpha-Lipoic Acid
Direct

Abstract PDF
HRP0086P1-P337

46,XY Partial Gonadal Dysgenesis Caused by an Xp21.2 Interstitial Duplication that Does not Encompass the NR0B1 Gene
Direct

Abstract PDF
HRP0086P1-P338

Primary Ovarian Insufficiency in Childhood Cancer Survivors: A Report from the St Jude Lifetime Cohort (SJLIFE)
Direct

Abstract PDF
HRP0086P1-P339

Global and Sexual Quality of Life in Patients with Rokitanski Syndrome: A Comparative Study Between Surgical vs Non Surgical Management of Vaginal Agenesis in a French Cohort of 130 Patients
Direct

Abstract PDF
HRP0086P1-P340

Intrauterine Growth Restriction Affects Postnatal Testis Maturation in Rats
Direct

Abstract PDF
HRP0086P1-P341

Application of on Line Learning in Assessment of Competencies of Fellows Pediatric Endocrinology
Direct

Abstract PDF
HRP0086P1-P342

Genotype-phenotype Analysis of NR5A1/SF1 Mutations by Functional in vitro Studies
Direct

Abstract PDF
HRP0086P1-P343

Evolution of Bone Mass and Body Composition in Gender Dysphoric Adolescents Treated with Progestins to Suppress Endogenous Hormones
Direct

Abstract PDF
HRP0086P1-P344

Sertoli Cell Function During Chemotherapy in Pediatric Patients with Acute Lymphoblastic Leukemia
Direct

Abstract PDF
HRP0086P1-P345

Accuracy of Pelvic MRI in Evaluating Internal Genitalia in Patients with Disorders of Sex Development
Direct

Abstract PDF
HRP0086P1-P346

Using Public Databases, 'Virtual Controls' and Geolocalization to Search for Environmental Correlates of Hypospadias
Direct

Abstract PDF
HRP0086P1-P347

The International AGD Consortium: A Multi-center Study of 3939 Infants and Children with Anogenital Distance Measurements
Direct

Abstract PDF
HRP0086P1-P348

Exonic Splicing Mutations by Silent Nucleotide Variation in the Androgen Receptor Gene Causes Androgen Insensitivity Syndrome
Direct

Abstract PDF
HRP0086P1-P349

Severe 5 Alpha Reductase 2 Deficiency with Aphallia is Caused by p.Y91H SRD5A2 Mutation and is Responsive to Dihydrotestosterone Administration During Childhood
Direct

Abstract PDF
HRP0086P1-P350

Clinical History and High Prevalence of Gonadal Tumor in 14 Patients with 46 XY Pure Gonadal Dysgenesis
Direct

Abstract PDF
HRP0086P1-P352

A Multicenter Study on Long-Term Outcomes in 56 Males with 45,X/46,XY Mosaicism
Direct

Abstract PDF
HRP0086P1-P353

Familial Testotoxicosis: Outcome and Possible Relation to Testicular Malignancies
Direct

Abstract PDF
HRP0086P1-P354

Psychological Impact in Young Women of Announcement of a Utero-Vaginal Malformation (Mayer-Rokitansky-Kuster-Hauser - MRKH Syndrome) and its Treatment
Direct

Abstract PDF
HRP0086P1-P355

Mutations at the SF-1 Ligand-Binding Domain Can Lead to Different Effects on DNA Binding: Report of Two Novel Mutations
Direct

Abstract PDF
HRP0086P1-P356

A New International Registry Highlights the Differences in Practice for Reaching a Diagnosis of CAH - On Behalf of the I-CAH/I-DSD Registry User Group
Direct

Abstract PDF
HRP0086P1-P357

Changes in Adrenal Steroids During Puberty Suppression and Cross Sex Hormone Treatment in Gender Dysphoric Adolescents
Direct

Abstract PDF
HRP0086P1-P358

Do the Anti-Mullerian Hormone Levels of Adolescents with Polycystic Ovarian Syndrome (PCOS), Those Who Are at Risk for Developing PCOS, and Those Who Exhibit Isolated Oligomenorrhea Differ from those of Adolescents with Normal Menstrual Cycles?
Direct

Abstract PDF
HRP0086P1-P359

Feasibility Study for Avoiding Early Surgery in Girls with 21-Hydroxylase Deficiency (21OHD)
Direct

Abstract PDF
HRP0086P1-P360

A Novel Familial Androgen Receptor Mutation (W752G) in Complete Androgen Insensitivity Syndrome: Use of in vitro Study According to the Nature of Amino Acid Substitution
Direct

Abstract PDF
HRP0086P1-P361

Partial and Mixed Gonadal Dysgenesis Cannot be Distinguished by Histological Picture: Clinical Evaluation, Histological Differences and Long-Term Follow up of 61 Brazilian Patients
Direct

Abstract PDF
HRP0086P1-P362

Aromatase Activity is Disrupted by Mutations in P450 Oxidoreductase
Direct

Abstract PDF
HRP0086P1-P363

Mosaic Xq Partial Duplication Leading to Virilisation of an Adolescent Female
Direct

Abstract PDF
HRP0086P1-P364

Genotyping Patients with Differences of Sex Development: 25 Years of Investigation of an Italian Population of 308 Cases (194 46,XY and 114 46,XX)
Direct

Abstract PDF
HRP0086P1-P365

Functional Studies of a New Mutation in the LH/CG Receptor Gene Identified in 2 Sisters with 46,XY DSD
Direct

Abstract PDF
HRP0086P1-P366

Consecutive Lynestrenol and Cross-Sex Hormone Treatment in Biological Female Adolescents with Gender Dysphoria: A Retrospective Analysis
Direct

Abstract PDF
HRP0086P1-P367

Ovarian Reserve Assessment in Girls and Women after Hematopoietic Stem Cell Transplantation Treatment Underwent in Childhood
Direct

Abstract PDF
HRP0086P1-P368

Precocious/Early and Accelerated Puberty in a Boy with a Homozygous R192C Mutation in CYP19 (Aromatase) Gene
Direct

Abstract PDF
HRP0086P1-P369

Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Accordingly Gender Assignment
Direct

Abstract PDF
HRP0086P1-P370

45,X/46,XY Chromosomal Disorders of Sex Development: Experience from a Cohort of 50 Patients Followed in One Single Institution
Direct

Abstract PDF
HRP0086P1-P371

Androgen Profile Differs to Adults in Adolescent Girls with Polycystic Ovary Syndrome
Direct

Abstract PDF
HRP0086P1-P372

Effects and Side Effects of Cyproterone Acetate Alone and in Combination with Estrogens in Natal Male Adolescents with Gender Dysphoria
Direct

Abstract PDF
HRP0086P1-P373

Compound Heterozygous C10orf2 Mutations in a Japanese Patient with 46,XX Ovarian Failure and Deafness
Direct

Abstract PDF
HRP0086P1-P374

GATA Transcription Factors in Testicular Adrenal Rest Tumours
Direct

Abstract PDF
HRP0086P1-P375

Can we Standardize Sex Assignment in 45,X/46,XY Mixed Gonadal Dysgenesis?
Direct

Abstract PDF
HRP0086P1-P376

Intratubular Large Cell Hyalinizing Sertoli Cell Tumor of the Testis Presenting with Prepubertal Gynecomastia: A Case Report
Direct

Abstract PDF
HRP0086P1-P377

Effect and Safety Aspects of Percutaneous Administration of Dihydrotestosterone in Children with Micropenis with Different Genetic Background
Direct

Abstract PDF
HRP0086P1-P378

Randomized Controlled Study Comparing Vitamin D and Omega 3-Fatty Acids Supplementation in Adolescents with Polycystic Ovary Syndrome
Direct

Abstract PDF
HRP0086P1-P379

Health-Related Quality of Life and Psychological Wellbeing in Adults with Diverse Sex Development
Direct

Abstract PDF
HRP0086P1-P380

Association of Genetic Polymorphisms Around the LIN28B Gene and Idiopathic Central Precocious Puberty Risks Among Chinese Girls
Direct

Abstract PDF
HRP0086P1-P381

Psychological Outcomes and Quality of Life of Patients with Non-CAH DSD
Direct

Abstract PDF
HRP0086P1-P382

Normalization of Ovulation Rate in Adolescent Girls with Hyperinsulinemic Androgen Excess
Direct

Abstract PDF
HRP0086P2-P383

Thyroid Autoimmunity in Adolescent Girls with Polycystic Ovary Syndrome - Pilot Study
Direct

Abstract PDF
HRP0086P2-P384

The Efficacy and Safety of Gonadotropin-Releasing Hormone Analogue Treatment to Suppress Puberty in Gender Dysphoric Adolescents
Direct

Abstract PDF
HRP0086P2-P385

A Familial form of DSD due to NR5A1 Mutation in a Father and His Son
Direct

Abstract PDF
HRP0086P2-P386

High Prevalence of SGA in Patients with Disorders of Sexual Development, Especially Idiopathic 46,XY DSD
Direct

Abstract PDF
HRP0086P2-P387

Questionnaire Surveys Targeting Japanese Pediatric Endocrinologists Regarding Reproduction in Pediatric and Adolescent Cancer Patients
Direct

Abstract PDF
HRP0086P2-P388

Fertility Outcomes after Childhood Onset Hypothalamic Hypogonadism
Direct

Abstract PDF
HRP0086P2-P389

Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia: A Novel AMH Receptor Mutation
Direct

Abstract PDF
HRP0086P2-P390

Three Cases of NR5A1 (SF1) Gene Mutations in DSD Patients
Direct

Abstract PDF
HRP0086P2-P391

Sertoli-Leydig Cell Tumor as a Rare Cause of Hirsutism in a Young Adolescent
Direct

Abstract PDF
HRP0086P2-P392

Identification of an AR Mutation in Klinefelter's Syndrome during Evaluation for Penoscrotal Hypospadias
Direct

Abstract PDF
HRP0086P2-P393

Assessment of Sexual Identity in Patients with Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P394

Duct Ectasia, a Rare Complication of Gynaecomastia
Direct

Abstract PDF
HRP0086P2-P395

Evaluation of Anti-Mullerian Hormone (AMH) Assay Roche® on Umbilical Cord Blood: Determination of Reference Values in Girls and Boys Newborn
Direct

Abstract PDF
HRP0086P2-P396

Hypogonadotropic Hypogonadism in a Girl with 2p11.2-2q12.1 Duplication
Direct

Abstract PDF
HRP0086P2-P397

A Nonvirilized form of Classic 3[beta]-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria
Direct

Abstract PDF
HRP0086P2-P398

Nonclassic Congenital Adrenal Hyperplasia and Functional Ovarian Hyperandrogenism Diagnosed During the Transition Period: Differences in Clinical, Hormonal and Metabolic Aspects
Direct

Abstract PDF
HRP0086P2-P399

Diagnosis of PCOS in Adolescents Using MRI
Direct

Abstract PDF
HRP0086P2-P400

Novel CYP17A1 Mutation and CYP21 Mutations in Two Siblings
Direct

Abstract PDF
HRP0086P2-P401

Aetiology of 46,XY DSD in Algeria; Putative Modifier Role of pV89L Polymorphism in the SRD5A2 Gene in Androgen Receptor Mutation-Negative Subjects
Direct

Abstract PDF
HRP0086P2-P402

Children with 46,XY DSD: Etiology, Clinical Profile, Socio-Demographic Details and Sex of Rearing
Direct

Abstract PDF
HRP0086P2-P403

Endocrine Risk Factors of Testicular Cancer of Children and Teenagers with Testicular Microlithiasis
Direct

Abstract PDF
HRP0086P2-P404

Case Report of a Girl with Secondary Amenorrhea Associated with Aurantiasis Cutis
Direct

Abstract PDF
HRP0086P2-P405

Maternal Ovarian Luteoma Causing Complete Virilization of a Female Fetus
Direct

Abstract PDF
HRP0086P2-P406

The Experience of GAIA (Abuse Childhood and Adolescence Group) - AOU Meyer
Direct

Abstract PDF
HRP0086P2-P407

State of Knowledge of Late Endocrinological Effects of Hematological Patients Who Has Undergone Chemotherapy
Direct

Abstract PDF
HRP0086P2-P408

Disorders of Sex Genitalia in Yaounde: Difficult Questions, Which Answers?
Direct

Abstract PDF
HRP0086P2-P409

Analysis of Clinical Manifestations and Gene Mutations of 5[alpha]-Reductase Type 2 Deficiency in 16 Cases
Direct

Abstract PDF
HRP0086P2-P410

Unusual Differential Diagnosis of Hyperandrogenism in Adolescent Female Treated for Polycystic Ovarian Syndrome
Direct

Abstract PDF
HRP0086P2-P411

Phenotypic and Hormonal Variability in 46,XY Subjects with SF-1 Mutations
Direct

Abstract PDF
HRP0086P2-P412

Towards the Roles of Kisspeptins in the Control of Gonadotropic Axis: Focus on Peripheral Signaling in Androgen-Dependent Tissues in the Experimentally Induced Model Hypogonadotropic Hypogonadism in Male Rats
Direct

Abstract PDF
HRP0086P2-P413

Two Patients Presenting the Extremes of the Phenotypic Spectrum of 5 alfa Reductase Deficiency: One with at New Mutation
Direct

Abstract PDF
HRP0086P2-P414

Disorders of Sex Development 45,X/46,XY: Clinical and Laboratory Characteristics of Patients
Direct

Abstract PDF
HRP0086P2-P415

Reproductive Function of Central Precocious Puberty in Girls: A Systematic Review
Direct

Abstract PDF
HRP0086P2-P416

Cytogenetic Variability and Phenotypic Findings in Patients with Ovotesticular Disorder of Sex development
Direct

Abstract PDF
HRP0086P2-P417

Cytogenetic Study of Sex Chromosomal Abnormalities in Egyptian DSD Patients
Direct

Abstract PDF
HRP0086P2-P418

Phenotype, Genotype and Gender Identity in Pubertal and Post-Pubertal Patients with Androgen Insensitivity Syndrome
Direct

Abstract PDF
HRP0086P2-P419

XLAG Syndrome Case Accompanying a New ARX Mutation and has a Interhemispheric Cyst
Direct

Abstract PDF
HRP0086P2-P420

Congenital Adrenal Lipoid Hyperplasia in a 30-Year-Old Female with a Tall Stature
Direct

Abstract PDF
HRP0086P2-P421

Onset of Puberty in Healthy Boys is Associated with a Decreased BMI Compared to Values Prior to the Onset of Puberty
Direct

Abstract PDF
HRP0086P2-P422

Late Clinical Presentation, Biological Assessment and Management of PAIS in a Developing Country
Direct

Abstract PDF
HRP0086P2-P423

Sisters with 46XY Gonadal Dysgenesis and Gonadoblastoma
Direct

Abstract PDF
HRP0086P2-P424

Follow-up to Adulthood of Two 46,XY Siblings with 5-alpha Reductase Deficiency and Different Sex of Rearing
Direct

Abstract PDF
HRP0086P2-P425

Constitutional Delay of Puberty: Clinical and Hormonal Characteristics of Patients
Direct

Abstract PDF
HRP0086P2-P426

Comparison between Serum Vitamin D Levels in Precocious Pubertal Girls and Normal Girls
Direct

Abstract PDF
HRP0086P2-P427

Complete Virilization without Salt Wasting in a 7-year-old Haitian Child with Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P428

Hematocolpos Revealed by Non-cyclic Lower-back Pain in a Pre-menarcheal Girl
Direct

Abstract PDF
HRP0086P2-P429

Novel AMH and AMHR-II Mutations in Two Egyptian Families with Persistent Mullerian Duct Syndrome
Direct

Abstract PDF
HRP0086P2-P430

Study of Genetics of Human Disorders of Sexual Development. Research Project.
Direct

Abstract PDF
HRP0086P2-P431

46XX Male Syndrome
Direct

Abstract PDF
HRP0086P2-P432

45,X/47,XYY Chromosomal Mosaicism as a Cause of 46,XY Disorder of Sex Development
Direct

Abstract PDF
HRP0086P2-P433

46,XY Complete Gonadal Dysgenesis with Late Diagnosis
Direct

Abstract PDF
HRP0086P2-P434

Diagnosis, Treatment and Gene Mutation Analysis of the Case with Steroid 5[alpha]-Reductase Type 2 Deficiency
Direct

Abstract PDF
HRP0086P2-P435

An Infant with 49XXXXY Syndrome: A Case Report from Sri Lanka
Direct

Abstract PDF
HRP0086P2-P436

Mixed Gonadal Disgenesia: Patients of Instituto da Crianca, HC-FMUSP
Direct

Abstract PDF
HRP0086P2-P437

Primary Amenorrhea as Alarm Manifestation in a Oligosymptomatic Girl with Xq Deletion and Turner Syndrome
Direct

Abstract PDF
HRP0086P2-P438

Hypogonadotropic Hypogonadism in a Patient with Vanishing Testis Syndrome - Case Report
Direct

Abstract PDF
HRP0086P2-P439

17 Alpha Hydroxylase, 17-20 Lyase Deficiency, a Case with Hypocalcemic Symptoms
Direct

Abstract PDF
HRP0086P2-P440

An Uncommon Case of Adolescent with POF
Direct

Abstract PDF
HRP0086P2-P441

Trisomy 9 Syndrome in an Infant with Ambiguous Genitalia
Direct

Abstract PDF
HRP0086P1-P442

Placental and Cord Blood DNA Methylation Profiling in Small-for-Gestational-Age Newborns from Uncomplicated Pregnancies: Relationship to Prenatal Growth and Postnatal Body Composition
Direct

Abstract PDF
HRP0086P1-P443

The Collapse of the BDNF/POMC System in the Hypothalamus is Responsible for the Extreme Obesity with Hyperphagia Observed in Female Heterozygous MeCP2 Null Mice
Direct

Abstract PDF
HRP0086P1-P444

Neonatal Overfeeding Alters Hepatic Insulin Sensitivity During Lactation and Leads to Long-term Insulin Resistance and Fatty Liver in Mice: Key Role of Mogat1
Direct

Abstract PDF
HRP0086P1-P445

The Impact of Activating PIK3CA Mutations and PTEN Haploinsufficiency on Human Adipocyte Phenotype and Biology
Direct

Abstract PDF
HRP0086P1-P446

Bioinactive Leptin is not Frequently Detected in Severe Early Onset Childhood Obesity
Direct

Abstract PDF
HRP0086P1-P447

Neonatal Overnutrition Causes Sex and Age Dependant Long-Term Effects on Body Weight, Body Composition and Serum Triglyceride and Free Fatty Acid Levels
Direct

Abstract PDF
HRP0086P1-P448

Laparoscopic sleeve gastrectomy in adolescents with morbid and dynamic obesity. A controlled monocentric study.
Direct

Abstract PDF
HRP0086P1-P449

Efficacy, Safety and Metabolic Effects of Carbohydrate Restriction in the Treatment of Obese Adolescents
Direct

Abstract PDF
HRP0086P1-P450

Severe Hypertriglyceridemia in Pediatric Oncology Patient
Direct

Abstract PDF
HRP0086P1-P451

The Frequencies of 5-HTTLPR Locus in Promotor Part of Serotonine Transporter Gene (SLC6A4) Polymorphism in Children with Different Forms of Obesity
Direct

Abstract PDF
HRP0086P1-P452

High Predictability of Impaired Glucose Tolerance by Combining Diagnostic Parameters in Obese Children
Direct

Abstract PDF
HRP0086P1-P453

The Effect of Subclinical Hypothyroidism (SH) and Treatment of SH with L-T4 on Basal Metabolic Rate in Obese Children: A Prospective Study
Direct

Abstract PDF
HRP0086P1-P454

Influence of Television Viewing During Meals on Eating Patterns
Direct

Abstract PDF
HRP0086P1-P455

Seven-year Follow-up of Mothers from a Randomized Controlled Trial of Exercise in Pregnancy and their Offspring
Direct

Abstract PDF
HRP0086P1-P456

E-Health: A National Registry and Therapeutic Algorithm for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence in Greece
Direct

Abstract PDF
HRP0086P1-P457

Premature Adrenarche and Metabolic Risk: Differences by Gender
Direct

Abstract PDF
HRP0086P1-P458

Association of miR-34a and mir-149 with Obesity and Insulin Resistance in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P1-P459

Erythropoietin Activates Classical Brown Adipose Tissue Through the Erythropoietin Receptor/STAT3 Pathway, Improving Obesity and Glucose Homeostasis in High Fat Diet-induced Obese Mice
Direct

Abstract PDF
HRP0086P1-P460

The Association between Insulin Resistance and Lower Extremity Muscle Strength, Static and Dynamic Standing Balances in Obese Adolescents
Direct

Abstract PDF
HRP0086P1-P461

Adiponectin and IL-6 in Simple Childhood Obesity with and without Hepatic Steatosis
Direct

Abstract PDF
HRP0086P1-P462

Determinants of Advanced Bone Age in Childhood Obesity
Direct

Abstract PDF
HRP0086P1-P463

Exposure to Phthalates Is Associated with Overweight or Obesity in 4-Year-Old Children
Direct

Abstract PDF
HRP0086P1-P464

Central Obesity among European Preschool Children: The ToyBox-Study
Direct

Abstract PDF
HRP0086P1-P465

Changes in Waist-to-Height Ratio during Preschool Years Differ between Children being Obese or Overweight at Five Years of Age Compared with not Overweight Children
Direct

Abstract PDF
HRP0086P1-P466

Remarkable Increase in the Prevalence of Overweight and Obesity among School Age Children in Antalya, Turkey, between 2003 and 2015
Direct

Abstract PDF
HRP0086P1-P467

The Peculiarities of Neurotransmitters Levels in Children with Obesity and Different Genotypes of COMT Gene
Direct

Abstract PDF
HRP0086P1-P468

Association of Fasting Triglycerides to High-Density Lipoprotein Ratio with Risk for Metabolic Disorders in Children
Direct

Abstract PDF
HRP0086P1-P469

Assessment of Adherence to Mediterranean Diet during a Weight Loss Intervention in Children with Cardiometabolic Risk
Direct

Abstract PDF
HRP0086P1-P470

Brain Structure, Executive Function and Appetitive Traits in Adolescent Obesity
Direct

Abstract PDF
HRP0086P1-P471

Improved Clinical and Laboratory Changes after 12 Months of Use of Metformin in Obese Insulin Resistant Children and Adolescents
Direct

Abstract PDF
HRP0086P1-P472

Risk factors for Atherosclerosis after Anticancer Treatment in Childhood: The Assessment of Lipid Parameters and Indicators of Susceptibility to Atherosclerosis in a Group of Pediatric Patients after Anticancer Treatment
Direct

Abstract PDF
HRP0086P1-P473

Inherited Duplication (X) (p11.4) Associated with Obesity, Autoaggressive Behaviour and Delayed Speech Development
Direct

Abstract PDF
HRP0086P1-P474

Switching Patients with Congenital Hyperinsulinism from Standard Octreotide to Long-Acting Release Octreotide Preserves Blood Glucose Control and Improves Quality of Life of Their Caregivers
Direct

Abstract PDF
HRP0086P1-P475

Reduction of Body Mass and Change in Body Composition of the Participants of the PoZdro! - Programme for Prevention of Diabetes and Civilisation Diseases by Medicover Foundation - Preliminary Results, after the First Year of Interventions
Direct

Abstract PDF
HRP0086P1-P476

Polysomnography in Obese Children with and without Prader-Willi
Direct

Abstract PDF
HRP0086P1-P477

Renal Involvement ın Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P1-P478

BMI Correlates Positively with Hair Cortisol, whereas Excessive Body Fat Correlates Positively with Hair Cortisol: Salivary Cortisol and Fasting Insulin Concentrations in Prepubertal Girls
Direct

Abstract PDF
HRP0086P1-P479

Hepatic Steatosis and Cardiovascular Risk in Overweight Children: Preliminary Results of the Study EFIGRO
Direct

Abstract PDF
HRP0086P1-P480

Associations of Different Appetite Hormones with Physical Activity and Cardiorespiratory Fitness in Adolescent Boys with Different BMI Values
Direct

Abstract PDF
HRP0086P1-P481

The Relation of Glycaemic Variability Obtained by Continuous Subcutaneous Glucose Monitoring with IL-6 and Adiponectin Levels in Obese Children with Metabolic Syndrome and Insulin Resistance
Direct

Abstract PDF
HRP0086P1-P482

Changes in Urine and Plasma Metabolomics Profiles after a Lifestyle Intervention Program in Obese Prepubertal Children
Direct

Abstract PDF
HRP0086P1-P483

The Effectiveness of a Stress Management Intervention Program in the Management of Overweight and Obesity in Childhood and Adolescence
Direct

Abstract PDF
HRP0086P1-P484

Fetuin-A as an Alternative Marker for Insulin Resistance and Cardiovascular Risk in Prepubertal Children
Direct

Abstract PDF
HRP0086P1-P485

What are Early Predictors of Impaired Glucose Tolerance in Children Born SGA?
Direct

Abstract PDF
HRP0086P1-P486

Multidisciplinary Intervention Programme in Childhood Obesity- Review of Service
Direct

Abstract PDF
HRP0086P1-P487

Hypercholesterolemia in Childhood: How the Response to Diet could Lead to Diagnosis. Lesson from a Case-Report
Direct

Abstract PDF
HRP0086P1-P488

Glucose Metabolism In Children with Prader-Willi Syndrome: The Effect Of Gh Therapy
Direct

Abstract PDF
HRP0086P1-P489

Impact of a Group-based Treatment Program on Adipocytokines, Oxidative status, Inflammatory Cytokines, and Pulse Wave Velocity in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P490

Matsuda Index in Correlation with Clinical Indicators of Insulin Resistance in Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P491

Anthropometric, Biological and Imagistical Methods For Assessing the Cardiovascular Risk in Obese Children
Direct

Abstract PDF
HRP0086P2-P492

Trends of Nutrition of Ukrainian Children from Kharkiv Region: Tendency to Overweight, Dehydration, Impaired Social Adaptation
Direct

Abstract PDF
HRP0086P2-P493

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P494

Comparison between CDC (Centers for Disease Control and Prevention) and Italian Growth Charts in the Characterization of Pediatric Obesity
Direct

Abstract PDF
HRP0086P2-P495

The Cutoff Values of Indirect Indices for Measuring Insulin Resistance in Korean Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P496

Intensive Exercise Intervention for Long-term Adolescent and Young Adult Survivors of Oncology-Related Cranial Insult: A Pilot Study
Direct

Abstract PDF
HRP0086P2-P497

Cardiometabolic Effect of Sugar-Sweetened Beverages Reduction in Obese Children
Direct

Abstract PDF
HRP0086P2-P498

A Comprehensive and Multidisciplinary Management Plan is Extremely Effective at Reducing the Prevalence of Overweight and Obesity in Childhood and Adolescence
Direct

Abstract PDF
HRP0086P2-P499

Multidisciplinary Care Management of Pediatric Obesity and Factors Associated with Better Outcomes
Direct

Abstract PDF
HRP0086P2-P500

Prevalence and Characteristics of Polycystic Ovary Syndrome in Obese Adolescents
Direct

Abstract PDF
HRP0086P2-P501

Efficacy of the Treatment for Childhood Obesity in Specialist Care: Age Over 10 Years at Baseline and Acanthosis Nigricans Predict a Worse Outcome
Direct

Abstract PDF
HRP0086P2-P502

Metabolic Syndrome in Prepubertal Obese Children: Inclusion of the Triglyceride/Hdl Ratio as an Alternative Diagnostic Criterion
Direct

Abstract PDF
HRP0086P2-P503

The relationship between Subclinical Hypothyroidism and Iodine Deficiency, Serum Leptin Levels and Metabolic Syndrome in Obese Children
Direct

Abstract PDF
HRP0086P2-P504

Analysis of Circulating miRNAs in Obese Children Born Small for Gestational Age
Direct

Abstract PDF
HRP0086P2-P505

Irisin and Abdominal Obesity in Preschool Age
Direct

Abstract PDF
HRP0086P2-P506

Long Term Outcomes after Hospital Based, Life-Style Weight Loss Intervention During Childhood
Direct

Abstract PDF
HRP0086P2-P507

Implications of Insulin Resistance in Obese and Overweight Children: A Cohort Analysis
Direct

Abstract PDF
HRP0086P2-P508

Effects of Highly Mineralized Water on Weight and Metabolism - A Randomized Controlled Blinded Trial in a Pediatric Hospital Staff
Direct

Abstract PDF
HRP0086P2-P509

Which Marker is the Most Reliable One for the Detection of NAFLD in Outpatient Clinic?
Direct

Abstract PDF
HRP0086P2-P510

Nonalcoholic Fatty Liver Disease: Evolution after 1 year of Follow-Up with Different Therapies
Direct

Abstract PDF
HRP0086P2-P511

Lifestyle Survey of Doctors, Medical Residents and Medical Students in Latvia
Direct

Abstract PDF
HRP0086P2-P512

Weight Status in Children at 8 Years: A Prospective Cohort Study
Direct

Abstract PDF
HRP0086P2-P513

Low Birth Weight is not Associated with Increased Risk of Metabolic Syndrome in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P514

Prader Willi Syndrome in Brazil: 6 months Follow-up in a Reference Center
Direct

Abstract PDF
HRP0086P2-P515

Early Blood Pressure Abnormalities Related to Cardiovascular Risk in Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P516

4G Polymorphism of Plasminogen Activator Inhibitor-1 (PAI-1), PAI-1 Plasma Levels, and Lipid Profiles in Overweight/Obese Children and Adolescents
Direct

Abstract PDF
HRP0086P2-P517

Polycystic Ovarian Syndrome in a Population of Obese Adolescents
Direct

Abstract PDF
HRP0086P2-P518

Vitamin D Deficiency in Obese Children and the Relationship with Insulin Resistance and Metabolic Syndrome
Direct

Abstract PDF
HRP0086P2-P519

Dietary Habits of Children and Adolescents Attending an Out-Patient Clinic for the Prevention and Management of Overweight and Obesity in Greece
Direct

Abstract PDF
HRP0086P2-P520

Preliminary Findings on Nutrition Care Competence in Health Care Professionals Using a Standardized Questionnaire NUTCOMP Korean Version
Direct

Abstract PDF
HRP0086P2-P521

Construction of Remote Monitoring System of Children with Tall or Short Stature and Overweight or Poor Weight Gain from the Elementary School Health Checkup Data
Direct

Abstract PDF
HRP0086P2-P522

The Effect of Demographic and Lifestyle Factors on One-year BMI Increments in 776 Norwegian Children Aged 6-15 Years
Direct

Abstract PDF
HRP0086P2-P523

Body Image Perception Changes in Obese and Lean Children
Direct

Abstract PDF
HRP0086P2-P524

Non-Alcoholic Hepatic Steatosis in Obese Children and the Relationship with Insulin Resistance
Direct

Abstract PDF
HRP0086P2-P525

Prevalence of Melanocortin 4 Receptor Mutations in Turkish Obese Children
Direct

Abstract PDF
HRP0086P2-P526

Prevalence of Overweight and Obesity in Children and Adolescents in Izmir, Western Turkey
Direct

Abstract PDF
HRP0086P2-P527

Arbitrary Cutoffs Lead to Underestimation of Metabolic Abnormalities in Obese Children: The Value of Age- and Sex-adjusted Normative Values
Direct

Abstract PDF
HRP0086P2-P528

Breasts Diseases in Adolescent Girls With Obesity
Direct

Abstract PDF
HRP0086P2-P529

Insulin Resistance Correlates to Cognitive Fatigue Dimensions in Non-diabetic Obese Children
Direct

Abstract PDF
HRP0086P2-P530

Vascular Endothelial Growth Factor as The Predictor Microangiopathy in Obese and Diabetic Children
Direct

Abstract PDF
HRP0086P2-P531

Associations of Serum 25-Hydroxyvitamin D and Components of the Metabolic Syndrome in an Egyptian Cohort
Direct

Abstract PDF
HRP0086P2-P532

Retrospective Evaluation of the Efficiency of Metformin Therapy in Obese Children with Insulin Resistance
Direct

Abstract PDF
HRP0086P2-P533

Parental Obesity can Trigger Obesity in Children
Direct

Abstract PDF
HRP0086P2-P534

Value of BMI-SDS, Waist Circumference-SDS and Waist-to-Height Ratio in the Identification of Obese Children and Adolescents at an Increased Risk for Cardio-Metabolic Complications
Direct

Abstract PDF
HRP0086P2-P535

Thyroid Dysfunction and Formation of Dyslipoproteiniaemias: Gender Differences in Children with Obesity
Direct

Abstract PDF
HRP0086P2-P536

How Early is Insulin Resistance in Our Pediatric Population with Metabolic Syndrome
Direct

Abstract PDF
HRP0086P2-P537

Insulin Resistance for Adolescents with Obesity in Latvia
Direct

Abstract PDF
HRP0086P2-P538

Parental Obesity can Trigger Obesity in Children
Direct

Abstract PDF
HRP0086P2-P539

Cerebrotendinous Xanthomatosis: A Case Report of Rare Lipid Storage Disorder
Direct

Abstract PDF
HRP0086P2-P540

Analysing Child Obesity Risk Factors: Adenotonsillectomy
Direct

Abstract PDF
HRP0086P2-P541

Non-Medicament Treatment of Severe Obese Children, Using the One-Year Courses
Direct

Abstract PDF
HRP0086P2-P542

Obstructive Sleep Apnea Syndrome in Early Childhood: Case Report
Direct

Abstract PDF
HRP0086P2-P543

25-Hydroxyvitamin D Concentrations in Pubertal Children with Obesity
Direct

Abstract PDF
HRP0086P2-P544

Management Preschool Children of Prader-Willi Syndrome
Direct

Abstract PDF
HRP0086P2-P545

Prevalence of Acanthosis Nigricans and Related Factors in Iranian Obese Children
Direct

Abstract PDF
HRP0086P1-P546

Higher Risk of Low Birth Weight and Multiple Nutritional Deficiencies in Neonates from Mothers after Gastric Bypass: A Case Control Study
Direct

Abstract PDF
HRP0086P1-P547

Laboratory Findings of 302 Patients with Hyperinsulinemic Hypoglycemia at Hypoglycemia
Direct

Abstract PDF
HRP0086P1-P548

Recognition of a Sequence: More Growth before Birth, Longer Telomeres at Birth, More Lean Mass after Birth
Direct

Abstract PDF
HRP0086P1-P549

Congenital Hyperinsulinism in Infancy: The Profiles of Insulin Secretory Granules are Markedly Different in Focal- and Diffuse [beta]-Cells
Direct

Abstract PDF
HRP0086P1-P550

Persistent Ketotic Hypoglycemia as an Atypical Presentation of Heterozygous HNF4A Mutation
Direct

Abstract PDF
HRP0086P1-P551

Enhanced Mitochondrial Densities Associate with the Pathobiology of [beta]-Cells in Congenital Hyperinsulinism in Infancy
Direct

Abstract PDF
HRP0086P1-P552

Congenital Adrenal Hyperplasia Newborn Screening: Improving the Effectiveness of the Neonatal 17OH-Progesterone and Serum Confirmatory Tests
Direct

Abstract PDF
HRP0086P1-P553

Neonatal Diabetes in Ukraine
Direct

Abstract PDF
HRP0086P1-P554

Clinical and Molecular Characteristics of Turkish Patients with Congenital Hyperinsulinism: A Single-Center Experience
Direct

Abstract PDF
HRP0086P1-P555

Islet of Langerhans in Congenital Hyperinsulinism in Infancy are Disrupted and with Decreased Expression of Collagen (IV) [alpha]1 Chain in Basement Membranes
Direct

Abstract PDF
HRP0086P1-P556

Pancreatic Glucagon Secretion is Severely Impaired and Somatostatin Secretion Unchanged in Patients with Hyperinsulinaemic Hypoglycaemia
Direct

Abstract PDF
HRP0086P1-P557

Mutations in MODY Genes: About Four Cases of Congenital Hyperinsulinism
Direct

Abstract PDF
HRP0086P1-P558

Cerebral Outcome of Children with Congenital Hyperinsulism
Direct

Abstract PDF
HRP0086P1-P559

Recognition of the Fetal and Perinatal Features of the Prader-Willi Syndrome is Required to Avoid Delay in Diagnosis
Direct

Abstract PDF
HRP0086P1-P560

Congenital Hyperinsulinism Due to Compound Heterozygous Mutation in ABCC8 and KCNJ11 GENES: 20 Years Experience of A National Referral Centre
Direct

Abstract PDF
HRP0086P1-P561

A Case of Hyperinsulinemic Hypoglycemia, Associated with Insulin Autoimmune Syndrome (IAS) in 3.5 Year Old Girl
Direct

Abstract PDF
HRP0086P1-P562

Effectiveness of Calcium Channel Blocker Nifedipine in Children with Hyperinsulinaemic Hypoglycaemia Due to Genetically Proven Mutations in the ABCC8/KCNJ11/GCK Genes
Direct

Abstract PDF
HRP0086P1-P563

Hyponatremia in Infants Under 100 Days Old: Frequently Overlooked and Multifactorial
Direct

Abstract PDF
HRP0086P1-P564

Long-Term Effects of Differences in Fetal Environment: Endocrine Influences on Cognitive Function and Personality in Teen Monozygotic Twins
Direct

Abstract PDF
HRP0086P1-P565

Different Long-term Neurodevelopmental Outcomes in Very Preterm Versus Very-low-birth-weight Infants
Direct

Abstract PDF
HRP0086P1-P566

Challenging Management of Costello Syndrome with Severe Congenital Hyperinsulinaemic Hypoglycaemia
Direct

Abstract PDF
HRP0086P1-P567

Risk Factors and Clinical Features of a Large Cohort of Patients with Transient Hyperinsulinemic Hypoglycaemia
Direct

Abstract PDF
HRP0086P1-P568

A Rare Case of Neonatal Hypothyroidism
Direct

Abstract PDF
HRP0086P1-P569

Maternal Nutritional Risk Factors Associated with Neonatal Hyperinsulinism
Direct

Abstract PDF
HRP0086P2-P570

Genotype and Phenotype of 99 Vietnamese Patients with Congenital Hyperinsulinism
Direct

Abstract PDF
HRP0086P2-P571

The Effects of Serum Insulin, Leptin, Ghrelin, Adiponectin and Resistin Levels on Early Postnatal Growth in Small for Gestational Age Newborns
Direct

Abstract PDF
HRP0086P2-P572

Sirolimus Therapy in Infant with Congenital Hyperinsulinemic Hypoglycemia Unresponsive to Diaxoside
Direct

Abstract PDF
HRP0086P2-P573

IPEX Syndrome Caused by A Novel Mutation in Foxp3 Gene: A Case Report
Direct

Abstract PDF
HRP0086P2-P574

Use of a Cord Blood F-Dex Monocyte Binding Assay to Study the Glucocorticoid Sensitivity in Premature Neonates
Direct

Abstract PDF
HRP0086P2-P575

Persistent Hyperinsulinemic Hypoglycemic of Infancy
Direct

Abstract PDF
HRP0086P2-P576

The Postnatal Effect of Serum Vitamin D Binding Protein on Serum Vitamin D Level
Direct

Abstract PDF
HRP0086P2-P577

Endocrinologists Have A Role in Moderating Adverse Metabolic Consequences of Early Over Feeding of Children Born IUGR
Direct

Abstract PDF
HRP0086P2-P578

Primary Hyperparathyroidism in Children and Adolescents: About a Series of Ten Patients
Direct

Abstract PDF
HRP0086P2-P579

The Effects of Serum Leptin, Ghrelin, Adiponectin and Resistin Levels on Early Postnatal Growth in Infants of Diabetic Mothers
Direct

Abstract PDF
HRP0086P2-P580

Newborns of Mothers Affected by Autoinmune Thyroid Disease
Direct

Abstract PDF
HRP0086P2-P581

Missense Mutation of GLIS3 Gene Resulting Inneonatal Diabetes and Congenital Hypothyroidism
Direct

Abstract PDF
HRP0086P2-P582

Birth Chest Circumference Relations to Circulating Insulin-Like Growth Factor-I in the Not-life-threatened Newborn: Relevance of Birthweight to Birth Crown-Heel Length Ratio Beyond The Presence of a Small Birthweight for Gestational Age and of Respiratory Support Measures
Direct

Abstract PDF
HRP0086P2-P583

Neonatal Failure to Thrive and Dyselectrolytemia - Not Always a Congenital Adrenal Hyperplasia
Direct

Abstract PDF
HRP0086P2-P584

A Unique IL2RA Mutation Presenting as Neonatal Diabetes, Congenital Hypothyroidism and Sepsis
Direct

Abstract PDF
HRP0086P2-P585

Change Level of TRAb in Newborn Leads to Thyroid Dysfunction - Case Report
Direct

Abstract PDF
HRP0086P2-P586

Hyperthyrotropinemia of the Preterm Newborn: Treat or Not to Treat?
Direct

Abstract PDF
HRP0086P2-P587

Permanent Neonatal Diabetes Mellitus Due to a G32S Heterozygous Mutation in the Insulin Gene
Direct

Abstract PDF
HRP0086P2-P588

Case Report on Hyperinsulinism/hyperammonaemia Syndrome: An Easily Treatable Cause of Postprandial Hypoglycaemia
Direct

Abstract PDF
HRP0086P2-P589

Severe Systemic Pseudohypoaldosteronism Type 1: 5 Years of Evolution
Direct

Abstract PDF
HRP0086P2-P590

Birth Chest Circumference Relations to Circulating Insulin-Like Growth Factor Binding Protein-3 in The Not-Life-Threatened Newborn: Relevance of Birthweight to Birth Crown-Heel Length Ratio After Control for A Small Birthweight for Gestational Age, for Respiratory Support Measures and for Circulating Insulin-Like Growth Factor-I
Direct

Abstract PDF
HRP0086P2-P591

Renal form of Pseudohypoaldosteronism Type I in Sucking: Clinical Case
Direct

Abstract PDF
HRP0086P2-P592

Neonatal Hyperparathyroidism with Homozygous Missense Mutation in the CASR Gene
Direct

Abstract PDF
HRP0086P1-P593

The Mechanistic Role of Fibroblast Growth Factor 21 (FGF21) in Growth Hormone Resistance Secondary to Chronic Childhood Conditions
Direct

Abstract PDF
HRP0086P1-P594

Somapacitan, a Once-Weekly Reversible Albumin-Binding Growth Hormone (GH) Derivative, Is Well Tolerated and Convenient in Adults with GH Deficiency (AGHD): Results from a 26-Week Randomised, Controlled Phase 3 Trial
Direct

Abstract PDF
HRP0086P1-P595

The Diagnostic Value of IGF-II, IGF-I and IGFBP-3 in Silver-Russell Syndrome
Direct

Abstract PDF
HRP0086P1-P596

Functional in vitro Characterization of Two Novel Germinal STAT3 Mutations Associated with Short Stature, Immunodeficiency and Autoimmune Disease
Direct

ESPE Abstracts

55th Annual ESPE