ESPE Abstracts

ESPE Abstracts

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55th Annual ESPE (ESPE 2016)

Paris, France
10 Sept 2016 - 12 Sept 2016

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Paris, France: 10-12 September 2016 Further information

Poster Presentations

Syndromes: Mechanisms and Management P2

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Syndromes: Mechanisms and Management P1
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Thyroid P1

hrp0086p2-p834 | Syndromes: Mechanisms and Management P2

Auxological Features in Patients with Vernal Keratoconjunctivitis

hrp0086p2-p835 | Syndromes: Mechanisms and Management P2

Turner Syndrome: Does GH Treatment Influence Glucose Homeostasis?

hrp0086p2-p836 | Syndromes: Mechanisms and Management P2

Renal Anomalies in Children with Turner Syndrome: Experience from a Single-Centre

hrp0086p2-p837 | Syndromes: Mechanisms and Management P2

Abstract unavailable

hrp0086p2-p838 | Syndromes: Mechanisms and Management P2

A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in Korean Girl

hrp0086p2-p839 | Syndromes: Mechanisms and Management P2

Evaluation of Referrals for Short Stature to a Regional Paediatric Centre

hrp0086p2-p840 | Syndromes: Mechanisms and Management P2

Testosterone Therapy Improves the First Year Height Velocity in Adolescent Boys with Constitutional Delay of Growth and Puberty

hrp0086p2-p841 | Syndromes: Mechanisms and Management P2

Safety and Efficacy of Growth Hormone (GH) in Combination with the Gonadotrophin Releasing Hormone Agonist Leuprorelin in Pubertal Children with Idiopathic Short Stature

hrp0086p2-p842 | Syndromes: Mechanisms and Management P2

Linear Growth in Infants and Children with Atopic Dermatitis

hrp0086p2-p843 | Syndromes: Mechanisms and Management P2

The Specific Pubertal Height Gain is Higher in Boys as Well as in Children with Lower BMISDS

hrp0086p2-p844 | Syndromes: Mechanisms and Management P2

Growth Screening in Children Aged Three to Five Years Seen in Community Paediatrics in Dreux District, France: Preliminary Results

hrp0086p2-p845 | Syndromes: Mechanisms and Management P2

The 3M Syndrome: A Cause of Pre- and Post-Natal Severe Growth Retardation

hrp0086p2-p846 | Syndromes: Mechanisms and Management P2

Should We Construct Specific Growth Charts for Ethnic Subgroups?

hrp0086p2-p847 | Syndromes: Mechanisms and Management P2

Late Presenting Girls with Turner Syndrome can Achieve a Normal Final Height

hrp0086p2-p848 | Syndromes: Mechanisms and Management P2

Growth of Children Born Preterm During the First 8 Years of Life

hrp0086p2-p849 | Syndromes: Mechanisms and Management P2

Genetic Variability in Patients with Noonan Syndrome in the Republic of Macedonia

hrp0086p2-p850 | Syndromes: Mechanisms and Management P2

An Unusual Cause of Short Stature in a Phenotypic Male with Type I Diabetes Mellitus due to an Unexpected Deletion of the Y Chromosome

hrp0086p2-p851 | Syndromes: Mechanisms and Management P2

An Unusual Case of Growth Hormone Replacement Therapy in a Child with Hereditary Multiple Exostoses and Growth Hormone Deficiency

hrp0086p2-p852 | Syndromes: Mechanisms and Management P2

Assessment of the Medical and Psychological Status of Women with Turner-Syndrome in Young Adulthood

hrp0086p2-p853 | Syndromes: Mechanisms and Management P2

A 3-year-old Boy with Growth Hormone Deficiency and Clinical Features of Ritscher–Schinzel Syndrome

hrp0086p2-p854 | Syndromes: Mechanisms and Management P2

Growth Pattern, Response to GH Treatment and the Effects of Pubertal Spurt on Final Height in Patients Affected by RASopathies

hrp0086p2-p855 | Syndromes: Mechanisms and Management P2

The Usefulness of Magnetic Resonance Imaging of the Heart and Aorta in the Diagnostic Work-up in Girls with Turner Syndrome

hrp0086p2-p856 | Syndromes: Mechanisms and Management P2

A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene

hrp0086p2-p857 | Syndromes: Mechanisms and Management P2

A Case of Familial Silver-Russell Syndrome

hrp0086p2-p858 | Syndromes: Mechanisms and Management P2

Central Precocious Puberty in a Case of SOTOS Syndrome

hrp0086p2-p859 | Syndromes: Mechanisms and Management P2

Hypoglycaemia in Isolated GH Deficiency beyond Infancy

hrp0086p2-p860 | Syndromes: Mechanisms and Management P2

Referral Pattern of Children with Short Stature to a Pediatric Endocrine Clinic in Kuwait

hrp0086p2-p861 | Syndromes: Mechanisms and Management P2

The Effect of Iron Intervention on the Anthropometric Parameters: Pilot Study among Egyptian Preschool Children with Iron Deficiency Anemia

hrp0086p2-p862 | Syndromes: Mechanisms and Management P2

Dopamine Beta-Hydroxylase Deficiency Leading to Growth Hormone Deficiency

hrp0086p2-p863 | Syndromes: Mechanisms and Management P2

Quality of Life in Growth Hormone Treated Children and Adolescents with Growth Hormone Deficiency and Smallness for Gestational Age

hrp0086p2-p864 | Syndromes: Mechanisms and Management P2

Secretion of Somatostatin and Growth Hormone (GH) in Various Forms of Hereditary Pathology

hrp0086p2-p865 | Syndromes: Mechanisms and Management P2

Postnatal Growth and Factors Modifying it in Very Low Birth Weight Preterms (PT) with Bronchopulmonary Dysplasia (BPD)

hrp0086p2-p866 | Syndromes: Mechanisms and Management P2

Endocrine and Metabolic Parameters before Onset of rGH Treatment: Potential Predictive Factors of GH Response in Children Born SGA? Results from Cohort of Nancy

hrp0086p2-p867 | Syndromes: Mechanisms and Management P2

Growth Hormone Treatment in a Child with Trisomy 21 and Turner Mosaicism

hrp0086p2-p868 | Syndromes: Mechanisms and Management P2

Pubertal Development and Final Height in Some Rare Genetic Diseases

hrp0086p2-p869 | Syndromes: Mechanisms and Management P2

Growth Hormone Deficiency in a Patient with Ring Chromosome 18

hrp0086p2-p870 | Syndromes: Mechanisms and Management P2

Children with Down’s Syndrome Show Quantitative, Phenotypical and Functional Differences of Effector T-Cells Compared to Immunocompetent Controls

hrp0086p2-p871 | Syndromes: Mechanisms and Management P2

Cardiovascular Anomalies in Turner Syndrome

hrp0086p2-p872 | Syndromes: Mechanisms and Management P2

Metamemory in Turner Syndrome: A Study Comparing Episodic and Semantic Memory

hrp0086p2-p873 | Syndromes: Mechanisms and Management P2

A XO/XX Girl with Lack of Morphological UTS-Features, Short Stature and Precocious Puberty

hrp0086p2-p874 | Syndromes: Mechanisms and Management P2

Transverse Myelitis in Turner Syndrome

hrp0086p2-p875 | Syndromes: Mechanisms and Management P2

Tricho-Rhino-Phalangeal Syndrome Type I in a Girl with Growth Hormone Deficiency

hrp0086p2-p876 | Syndromes: Mechanisms and Management P2

Project Epi Peg-Premeb. Clinical Situation of a Person Born SGA Followed from Birth Cohort. GLOBAL Causes and Clinical Situation of Partial Birth Cohort and 12 Months

hrp0086p2-p877 | Syndromes: Mechanisms and Management P2

Pituitary Gigantism and Central Precocious Puberty Presenting with Prognathism in a Pediatric Patient

hrp0086p2-p878 | Syndromes: Mechanisms and Management P2

The Monitoring of Endocrine Functions in Children with Rare Genetic Syndromes

hrp0086p2-p879 | Syndromes: Mechanisms and Management P2

SHORT Syndrome and rhGH Treatment – Is It Useful?

hrp0086p2-p880 | Syndromes: Mechanisms and Management P2

Late Diagnosis of Mixed Gonadal Dysgenesis – Clinical and Psychological Implications

hrp0086p2-p881 | Syndromes: Mechanisms and Management P2

The Structure of Genetically Determined Types of Short Stature in Uzbekistan According to Retrospective Analysis

hrp0086p2-p882 | Syndromes: Mechanisms and Management P2

Evaluation of Growth Pattern in Prader-Willi Syndrome

hrp0086p2-p883 | Syndromes: Mechanisms and Management P2

Prader-Willi Syndrome – Different Patients, Different Attitude

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