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55th Annual ESPE

Paris, France
10 Sep 2016 - 12 Sep 2016

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Paris, France: 10-12 September 2016 Further information

Poster Presentations

Syndromes: Mechanisms and Management P2

Auxological Features in Patients with Vernal Keratoconjunctivitis
aHealth Science Department, University of Florence, Anna Meyer Children’s University Hospital, Florence, Italy; bPaediatric Allergology Unit, Anna Meyer Children’s University Hospital, Florence, Italy; cCRR Fibrosi Cistica e Celiachia, Atri Hospital, Atri, Teramo, Italy
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Turner Syndrome: Does GH Treatment Influence Glucose Homeostasis?
aDepartment of Pediatrics, Pediatric Endocrinology Program, University of Bologna and S. Orsola-Malpighi Hospital, Bologna, Italy; bDepartment of Pediatrics, Regional Hospital Bolzano, Bolzano, Italy
hrp0086p2-p835
Renal Anomalies in Children with Turner Syndrome: Experience from a Single-Centre
aDevelopmental Endocrinology Research Group, Royal Hospital for Children, University of Glasgow, Glasgow, UK; bPaediatric Unit, Department of Medical and Surgical Sciences for Mother, Children and Adults, University of Modena & Reggio Emilia, Modena, Italy; cDepartment of Pediatric Surgery, Royal Hospital for Children, Glasgow, UK
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Abstract unavailable
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A Novel Fibrillin-1 Gene Mutation Leading to Marfan Syndrome in Korean Girl
aDepartment of Pediatrics, College of Medicine, Korea University, Seoul, Republic of Korea; bDepartment of Laboratory Medicine, College of Medicine, Korea University, Seoul, Republic of Korea
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Evaluation of Referrals for Short Stature to a Regional Paediatric Centre
Children’s Hospital, London Health Sciences Centre, London, Ontario, Canada
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Safety and Efficacy of Growth Hormone (GH) in Combination with the Gonadotrophin Releasing Hormone Agonist Leuprorelin in Pubertal Children with Idiopathic Short Stature
aEndocrinology and Diabetes Unit, Eli Lilly, Neuilly-sur-Seine, France; bDepartment Endocrine, Bone Diseases, Genetics, Obesity, and Gynecology Unit, and INSERM UMR1043, Children’s Hospital, University Hospital, Toulouse, France; cBioclinica, Bessenay, France; dEli Lilly, Bad Homburg, Germany; eEli Lilly and Company, Indianapolis, USA; fDepartment of Pediatric Endocrinology and Diabetology, and INSERM U690, University Paris 7, Denis Diderot, Hôpital Robert Debré, Paris, France
hrp0086p2-p841
Linear Growth in Infants and Children with Atopic Dermatitis
aHamad Medical Center, Doha, Qatar; bUniversity of Alexandria, Alexandria, Egypt
hrp0086p2-p842
The Specific Pubertal Height Gain is Higher in Boys as Well as in Children with Lower BMISDS
aGPGRC, Department of Pediatrics, Intuition of Clinical Sciences, Sahlgrenska Academy, Gothenburg, Sweden; bDepartment of Pediatrics, Halmstad County Hospital, Halmstad, Sweden; cMuvara bv, Leiderdorp, The Netherlands; dDepartment of Food & Nutrition, & Sport Science, University of Gothenburg, Gothenburg, Sweden; eDepartment of Public Health & Community Medicine, Intuition of Medicine, The Sahlgrenska Academy, Gothenburg, Sweden; fDepartment of Physiology, Division of Endocrinology, Intuition of Neuroscience & Physiology, The Sahlgrenska Academy, Gothenburg, Sweden
hrp0086p2-p843
Growth Screening in Children Aged Three to Five Years Seen in Community Paediatrics in Dreux District, France: Preliminary Results
aPaediatric Endocrinology Unit, Department of Paediatrics, Victor Jousselin Hospital, Dreux, France; bService de Protection Maternelle & Infantile, Dreux, France; cClinical Research Unit, URC28, Dreux, France; dIPSEN Laboratories, Boulogne-Billancourt, France; eParis Descartes University, Paris, France
hrp0086p2-p844
The 3M Syndrome: A Cause of Pre- and Post-Natal Severe Growth Retardation
aIstanbul University, Istanbul Faculty of Medicine, Department of Pediatrics, Pediatric Endocrinology Unit, Istanbul, Turkey; bIstanbul University, Istanbul Faculty of Medicine, Department of Medical genetics, Istanbul, Turkey
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Should We Construct Specific Growth Charts for Ethnic Subgroups?
University of Medicine and Pharmacy Tirgu-Mures, Tirgu-Mures, Romania
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Late Presenting Girls with Turner Syndrome can Achieve a Normal Final Height
Department of Endocrinology and Diabetes, Birmingham Children’s Hospital, Birmingham, UK
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Growth of Children Born Preterm During the First 8 Years of Life
Department of Pediatrics, Universidade Federal do Parana, Curitiba, Parana, Brazil
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Genetic Variability in Patients with Noonan Syndrome in the Republic of Macedonia
aUniversity Pediatric Clinic, Skopje, Macedonia; bMedical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea
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An Unusual Case of Growth Hormone Replacement Therapy in a Child with Hereditary Multiple Exostoses and Growth Hormone Deficiency
aFirst Department of Pediatrics, P & A Kyriakou, Children’s Hospital, Athens, Greece, bDepartment of Medical Genetics, Athens University Medical School, Aghia Sophia Children’s Hospital, Athens, Greece
hrp0086p2-p851
A 3-year-old Boy with Growth Hormone Deficiency and Clinical Features of Ritscher-Schinzel Syndrome
aDepartment of Pediatrics, University Hospital “St. Marina”, Varna Medical University, Varna, Bulgaria; bDepartment of General Medicine and Clinical Laboratory, University Hospital “St. Marina”, Varna Medical University, Varna, Bulgaria; cDepartment of Pediatrics, University Pediatric Hospital, Sofia Medical University, Sofia, Bulgaria; dDepartment of Genetics, Dysmorphology, Metabolic Diseases, University Pediatric Hospital, Sofia Medical University, Sofia, Bulgaria; eDepartment of Imaging Diagnostics and Radiotherapy, University Hospital “St. Marina”, Varna Medical University, Varna, Bulgaria
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Growth Pattern, Response to GH Treatment and the Effects of Pubertal Spurt on Final Height in Patients Affected by RASopathies
Department of Pediatrics, Pediatric Endocrinology and Rare Diseases Unit, S.Orsola-Malpighi University Hospital-University of Bologna, Bologna, Italy
hrp0086p2-p854
The Usefulness of Magnetic Resonance Imaging of the Heart and Aorta in the Diagnostic Work-up in Girls with Turner Syndrome
aDepartment of Pediatric Endocrinology and Rheumatology, Poznan University of Medical Sciences, Poznan, Poland; b1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland; cDepartment of Pediatric Cardiology and Nephrology, Poznan University of Medical Sciences, Poznan, Poland
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A Rare Cause of Short Stature: Patient with 3M Syndrome Revealed a New Mutation in Osbl1 Gene
Dr. Sami Ulus Obstetrics and Gynecology and Pediatrics Training and Research Hospital, ANKARA, Turkey
hrp0086p2-p856
A Case of Familial Silver-Russell Syndrome
aDepartment of Paediatric Endocrinology, Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany; bExplorations Fonctionnelles Endocriniennes, Hôpital d’Enfants Armand-Trousseau, Paris, France; cInstitute of Human Genetics, University Hospital of Technology (RWTH) Aachen, Aachen, Germany; dInstitute of Human Genetics, University Hospital Leipzig, Leipzig, Germany
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Central Precocious Puberty in a Case of SOTOS Syndrome
Broomfield Hospital, Chelmsford, UK
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Hypoglycaemia in Isolated GH Deficiency beyond Infancy
KLinik für Kinder-und Jugendmedizin, Klinikum Bremen Nord, Bremen, Germany
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The Effect of Iron Intervention on the Anthropometric Parameters: Pilot Study among Egyptian Preschool Children with Iron Deficiency Anemia
aPediatric Department, DEMPU, Faculty of Medicine, Cairo University, Cairo, Egypt; bPediatric Department, Faculty of Medicine, Cairo University, Cairo, Egypt
hrp0086p2-p861
Dopamine Beta-Hydroxylase Deficiency Leading to Growth Hormone Deficiency
aDepartment of Pediatric Endocrinology, Ataturk University Faculty of Medicine, Erzurum, Turkey; bDepartment of Pediatrics, Ataturk University Faculty of Medicine, Erzurum, Turkey
hrp0086p2-p862
Quality of Life in Growth Hormone Treated Children and Adolescents with Growth Hormone Deficiency and Smallness for Gestational Age
aUZ Brussel, Brussel, Belgium; bUZ Gent, Gent, Belgium; cUZ Leuven, Leuven, Belgium; dUZ Antwerpen, Antwerpen, Belgium; eCHU Liège, Liège, Belgium; fCliniques Universitaires Saint Luc, Bruxelles, Belgium; gCliniques Universtaires Mont Godinne, Mont Godinne, Belgium; hHUDERF, Bruxelles, Belgium; iAZ Delta, Roeselare, Belgium; jAZ Sint Jan, Brugge, Belgium; kBESPEED, Brussels, Belgium; lVUB, Brussel, Belgium; mJessa ziekenhuis, Hasselt, Belgium
hrp0086p2-p863
Secretion of Somatostatin and Growth Hormone (GH) in Various Forms of Hereditary Pathology
Laboratory of Genomics under the Institute of Bioorganic Chemistry of the Republic of Uzbekistan Academy of Sciences, Tashkent, Uzbekistan
hrp0086p2-p864
Postnatal Growth and Factors Modifying it in Very Low Birth Weight Preterms (PT) with Bronchopulmonary Dysplasia (BPD)
aHamad Medical Center, Doha, Qatar; bCollege of Medicine University of Alexandria, Alexandria, Egypt
hrp0086p2-p865
Pubertal Development and Final Height in Some Rare Genetic Diseases
Pediatric Endocrinology and Rare Diseases Unit, Department of Pediatrics, S. Orsola-Malpighi University Hospital-University of Bologna, Bologna, Italy
hrp0086p2-p868
Growth Hormone Deficiency in a Patient with Ring Chromosome 18
Medical University of Gdansk, Clinic of Paediatrics, Diabetology and Endocrinology, Gdansk, Poland
hrp0086p2-p869
Children with Down's Syndrome Show Quantitative, Phenotypical and Functional Differences of Effector T-Cells Compared to Immunocompetent Controls
aDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany; bDepartment of Pediatrics and Neonatology, University Children’s Hospital of Saarland, Homburg, Germany; cDepartment of Pediatric Cardiology, University Children’s Hospital of Saarland, Homburg, Germany; dDivision of Pediatric Cardiology, University Children’s Hospital, Ulm, Germany
hrp0086p2-p870
Cardiovascular Anomalies in Turner Syndrome
aDepartment of Endocrinology Bologhine Hospital, Algiers, Algeria; bDepartment of Endocrinology Bab El Oued Hospital, Algiers, Algeria
hrp0086p2-p871
Metamemory in Turner Syndrome: A Study Comparing Episodic and Semantic Memory
aLaboratoire de Psychologie et Neurocognition, Grenoble, France; bLaboratoire d’étude de l’apprentissage et du développement, Dijon, France; cEndocrinology, Hospital, Besançon, France; dGenetics of Development Disorders, Dijon, France
hrp0086p2-p872
A XO/XX Girl with Lack of Morphological UTS-Features, Short Stature and Precocious Puberty
aKlinik für Kinder- und Jugendmedizin Klinikum Bremen Nord, Bremen, Germany; bMedical Practice, Lilienthal, Germany
hrp0086p2-p873
Transverse Myelitis in Turner Syndrome
aHospital Da Criança Santo Antônio, Porto Alegre, Brazil; bUniversidade De Ciências Da Saúde De Porto Alegre, Porto Alegre, Brazil
hrp0086p2-p874
Tricho-Rhino-Phalangeal Syndrome Type I in a Girl with Growth Hormone Deficiency
aMersin Maternity and Children Hospital Pediatric Endocrinology, Mersin, Turkey; bDepartment of Genetics, Mersin University, Mersin, Turkey
hrp0086p2-p875
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
aOSI Araba - Hospital Universitary of Alava - Peadiatric Endocrinology, Vitoria - Basque Country, Spain; bBasque Country University, Vitoria, Spain; cOSI Araba - Hospital Universitary of Alava - Peadiatric Neonatology, Vitoria, Spain; dGrupo Nutrición y Obesidad, Facultad de Farmacia, Universidad del, Vitoria, Spain; eCIBERObn, Instituto de Salud Carlos III. Madrid, Vitoria, Spain
hrp0086p2-p876
Pituitary Gigantism and Central Precocious Puberty Presenting with Prognathism in a Pediatric Patient
aRUSH University Medical Center, Chicago, IL, USA; bJohn Stroger Hospital of Cook County, Chicago, IL, USA
hrp0086p2-p877
The Monitoring of Endocrine Functions in Children with Rare Genetic Syndromes
aState Center for Medical Rehabilitation, Minsk, Belarus; bRegional Children Hospital, Kaliningrade, Russia; cBelarusian State Medical University, Minsk, Belarus
hrp0086p2-p878
SHORT Syndrome and rhGH Treatment - Is It Useful?
University of Medicine and Pharmacy “Gr.T Popa”, Iasi, Romania
hrp0086p2-p879
Late Diagnosis of Mixed Gonadal Dysgenesis - Clinical and Psychological Implications
aDepartment of Endocrinology, Iasi, Romania; bDepartment of Endocrinology, Bacau, Romania; cDepartment of Radiology, Iasi, Romania
hrp0086p2-p880
The Structure of Genetically Determined Types of Short Stature in Uzbekistan According to Retrospective Analysis
Laboratory of Genomics Under the Institute of Bioorganic Chemistry of Republic of Uzbekistan Academy of Sciences, Tashkent, Uzbekistan
hrp0086p2-p881
Evaluation of Growth Pattern in Prader-Willi Syndrome
Kirikkale University Faculty of Medicine, Kirikkale, Turkey
hrp0086p2-p882
Prader-Willi Syndrome - Different Patients, Different Attitude
aDepartment of Endocrinology, University of Medicine and Pharmacy “Gr. T. Popa” Iasi, Iasi, Romania; bDepartment of Genetics, University of Medicine and Pharmacy “Gr. T. Popa” Iasi, Iasi, Romania; cDepartment of Pneumology, University of Medicine and Pharmacy “Gr. T. Popa” Iasi, Iasi, Romania
hrp0086p2-p883