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57th Annual ESPE

Athens, Greece
27 Sep 2018 - 29 Sep 2018

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ESPE 2018 57th European Society for Paediatric Endocrinology Annual Meeting 27-29 September 2018 Athens, Greece

Poster Presentations

Adrenals and HPA Axis P2

Contribution of Direct Measurements of Steroids by Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS) in Non-classical Adrenal Hyperplasia (NCCAH)
aExplorations Fonctionnelles Endocriniennes, Centre de Reference des maladies Endocriniennes rares de la croissance et du Développement. Hôpital A Trousseau AP-HP, 26 av A Netter 75012, Paris, France; bPlateforme Peptidomique, Métabolomique et Dosage de Médicaments (PM2) Hôpital St Antoine 184 rue du Fbg St Antoine 75012, Paris, France; cSorbonne Université, INSERM U 938 University, Paris, France
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GnRH-analogue Treatment in Children with Congenital Adrenal Hyperplasia (CAH): Data from a Multicenter CAH Registry
aPediatric Endocrinology, Children’s Hospital, University of Bonn, Bonn, Germany; bCenter of Reproductive Medicine and Andrology, Department of Clinical Andrology, University of Muenster, Muenster, Germany; cPediatric Endocrinology, Department of Pediatrics, Helios Kliniken, Krefeld, Germany; dPediatric Endocrinology and Diabetology, Sana Klinikum Lichtenberg, Berlin, Germany; ePediatric Endocrinology, Department of Pediatrics, Evangelisches Krankenhaus Bielefeld, Bielefeld, Germany; fPediatric Endocrinology, Department of Pediatrics and Adolescent Medicine, University Medical Center, Freiburg, Germany; gPediatric Endocrinology, Department of Pediatrics, Klinikum rechts der Isar, Technische Universität München, Munich, Germany; hPediatric Endocrinology, Department of Pediatrics, Krankenhaus der Stadt Dornbirn, Dornbirn, Austria; iGermany
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Glucocorticoid Replacement Regimens in the Treatment of 21-hydroxylase Deficiency Congenital Adrenal Hyperplasia: A Systematic Cochrane Review
aSouthport and Ormskirk Hospitals NHS Trust, Southport, UK; bUniversity of Liverpool, Liverpool, UK; cSalford Royal NHS Foundation Trust, Salford, UK
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Hydrocortisone (HC) Dose in Children with Congenital Adrenal Hyperplasia (CAH)
aChildren’s Hospital, University of Cologne, Cologne, Germany; bChildren’s Hospital, University of Dresden, Dresden, Germany; cChildren’s Hospital, University of Muenster, Muenster, Germany; dPediatric Endocrinology Practice, Oldenburg, Germany; eChildren’s Hospital, University of Heidelberg, Heidelberg, Germany; fChildren’s Hospital, University of Homburg, Homburg, Germany; gChildren’s Hospital, University of Innsbruck, Innsbruck, Austria; hInstitute of Statistics, University of Magdeburg, Magdeburg, Germany; iInstitute of Epidemiology and Medical Biometry, Ulm, Germany; jChildren’s Hospital, University of Bonn, Bonn, Germany; kGermany
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Perioperative Care of CAH - Incongruencies of Practices among Canadian Specialists
aDivision of Pediatric Endocrinology, Department of Pediatrics, University of Saskatchewan, Saskatoon, Canada; bDepartment of Anesthesiology, Perioperative Medicine and Pain Management, University of Saskatchewan, Saskatoon, Canada; cClinical Research Support Unit, College of Medicine, University of Saskatchewan, Saskatoon, Canada
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Analysis of Phenotypes and Genotypes in 84 Patients with 21-hydroxylase Deficiency
Department of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China
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Miscarriages in Families with a Child with Classic Congenital Adrenal Hyperplasia and 21-Hydroxylase Deficiency (CAH)
aPediatric Endocrinology, Department of Pediatrics, University Hospital of Erlangen, Erlangen, Germany; bPediatric Gynecology, Department of Gynecology and Obstetrics, University Hospital of Erlangen, Erlangen, Germany.
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Testing Antiandrogens and Aromatase Inhibitors to Achieve Normal Growth in Children with Classical Congenital Adrenal Hyperplasia: A Systematic Review and Meta-analysis
aMaternity and Children Hospital, Dammam, Saudi Arabia; bNational & Gulf Center for Evidence Based Health Practice, Collage of Public Health, King Saud bin Abdul – Aziz University for Health Sciences, Riyadh, Saudi Arabia; cMidlink International, Collage of Public Health, Alexandria University, Alexandria, Egypt; dNational & Gulf Center for Evidence Based Health Practice, Collage of Public Health King Saud bin Abdul Aziz University for Health Sciences, Riyadh, Saudi Arabia
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Phenotype-genotype Correlations of CYP21A2 Mutations in Patients with Congenital Adrenal Hyperplasia in Turkey
aDepartment of Pediatrics, Division of Pediatric Endocrinology, Osmangazi University School of Medicine, Eskisehir, Turkey; bDepartment of Medical Genetics, Osmangazi University School of Medicine, Eskisehir, Turkey
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Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38 935 Infants
aTurkish Society for Paediatric Endocrinology and Diabetes, Istanbul, Turkey; bTurkish Directorate of Public Health, Ankara, Turkey
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A First Combination Case of 21-Hydroxilase Deficiency and CHARGE Syndrome Confirmed by Genetic Analysis
aDepartment of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Japan; bDepartment of Molecular Endocrinology, National Research Institute for Child Health, Tokyo, Japan
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Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients
Division of Pediatric Endocrinology and Metabolism, Health Sciences University, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
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Study of Cardiovascular Risk Factors and Carotid Intima-Media Thickness in Children with Congenital Adrenal Hyperplasia
aFaculty of medicine, Pediatric Endocrinology and Diabetology, Alexandria University Children’s Hospital, Alexandria, Egypt; bAlexandria University Children’s Hospital, Alexandria, Egypt; cFaculty of Medicine, Radiodiagnosis, Alexandria University, Alexandria, Egypt
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The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective Analysis
aSt George’s, University of London Medical School at the University of Nicosia, Nicosia, Cyprus; bDepartment of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus; cDivision of Pediatric Endocrinology, Paedi Center for specialized Pediatrics, Nicosia, Cyprus; dPediatric Endocrine Clinic, IASIS Hospital, Paphos, Cyprus; eDivision of Pediatric Endocrinology, Makarios III Hospital, Nicosia, Cyprus; fAlithias Endocrinology Center, Nicosia, Cyprus; gDasoupolis Endocrinology Center, Nicosia, Cyprus; hDevelopmental Endocrinology Research Group, School of Medicine, University of Glasgow, Glasgow, UK; iIliaktida Peadiatric & Adolescent Medical Centre, Limassol, Cyprus; jYale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA; kDepartment of Clinical Genetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus; lCyprus School of Molecular Medicine, Nicosia, Cyprus
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A Novel Mutation in the MC2R Gene in a Two-year-old Boy with Adrenal Insufficiency
Department of Pediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar
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Two Cases of Apparent Mineralocorticoid Excess due to Novel Mutations in HSD11B2 Gene
aEndocrinology Research Centre, Moscow, Russian Federation; bChildren’s Republic Hospital, Machachkala, Russian Federation
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Borderline Peak Plasma Cortisol Following Synacthen Stimulation - Single-centre Analysis of Three Years Data
aSheffield Children’s NHS Foundation Trust, Sheffield, UK; bThe Univeristy of Sheffield, Sheffield, UK
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Unilateral Adrenalectomy for Primary Pigmented Nodular Adrenocortical Disease Causing Cushing Syndrome
Division of Pediatric Endocrinology and Metabolism, Children’s Medical Center, Osaka City General Hospital, Osaka, Japan
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Adrenal Crisis in Children with Adrenal Insufficiency: Prevalence and Risk Factors
aPediatric Endocrinology Unit, Dana-Dwek Children’s Hospital, Tel-Aviv Medical Center, Tel Aviv, Israel; bSackler School of Medicine Tel-Aviv University, Tel Aviv, Israel; cPediatric Endocrinology Unit, Kaplan Medical Center, Rehovot, Israel; dThe Hebrew University of Jerusalem, Jerusalem, Israel; ePediatric Endocrinology Unit, Assaf Harofeh Medical Center, Zerifin, Israel; fPediatric Endocrinology Unit, Wolfson Medical Center, Holon, Israel
hrp0089p2-p023
The Effectiveness of a Stress-Management Intervention Program in Behavioral Parameters and Hair Cortisol Concentrations in Children with Attention Deficit Hyperactivity Disorder
aPostgraduate Course, Science of Stress Management and Health Promotion, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece; bDevelopmental & Behavioral Pediatrics Unit, First Department of Pediatrics, “Aghia Sophia” Children’s University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece; cChoremeion Research Laboratory, First Department of Pediatrics, “Aghia Sophia” Children’s University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece; dCenter for Differential Diagnosis, Diagnosis and Support (KE.D.D.Y.), Pyrgos, Greece
hrp0089p2-p024
Very High Dehydroepiandrosterone Sulfate (DHEAS) in Serum of an Overweight Female Adolescent without a Tumor
aUniversity Children’s Hospital, Tuebingen, Germany; bUniversity Children’s Hospital, Giessen, Germany; cInstitute for Pharmacology and Toxicology, Veterinary Medicine, Justus Liebig University, Giessen, Germany
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Early Recognition of Adrenal Insufficiency after Hematopoietic Stem Cell Transplantation During Childhood
Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, South Korea
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Reference Values for Serum 17-alfa Hydroxyprogesterone and Adrenal Size in Healthy Newborns
aDepartment of Pediatric Endocrinology, School of Medicine, Karadeniz Technical University, Trabzon, Turkey; bDepartment of Radiology, School of Medicine, Karadeniz Technical University, Trabzon, Turkey; cDepartment of Biochemistry, Akdeniz University School of Medicine, Antalya, Turkey; dDepartment of Neonatology, School of Medicine, Karadeniz Technical University, Trabzon, Turkey; eDepartment of Public Health, School of Medicine, Karadeniz Technical University, Trabzon, Turkey
hrp0089p2-p027
A Rare Case of ACTH-Independent Cushing's Syndrome due to Bilateral Micronodular Adrenal Hyperplasia and Myoclonic Dystonia
Division of Endocrinology, Diabetes and Metabolism, First Department of Pediatrics, National and Kapodistrian University of Athens Medical School, ‘Aghia Sophia’ Children’s Hospital, Athens, Greece
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Ganglioneuroma Presenting as an Adrenal Incidentaloma in a 10-year-old boy-a Rare Entity
Smt Kashibai Navale Medical College and General Hospital, Pune, India
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The Relationship Between Vitamin D Status and Metabolic Abnormalities in Females with Classical Congenital Adrenal Hyperplasia: A Pilot Study
aPediatric Department, DEMPU, Faculty of Medicine, Cairo University, Cairo, Egypt; bDepartment of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt; cPediatric Department, Faculty of Medicine, Cairo University, Cairo, Egypt
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Adrenal Hypoplasia Seemingly First as a Primary Hypoaldosteronism
aDepartment of Medical and Surgical Sciences of the Mother, Children and Adults. University of Modena and Reggio Emilia, Modena, Italy; bLaboratoire de Biochimie et Biologie Moléculaire Grand Est, UM Pathologies Endocriniennes Rénales Musculaires et Mucoviscidose, Groupement Hospitalier Est, Hospices Civils de Lyon, Univ Lyon, Lyon, France
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Etiology of Primary Adrenal Insufficiency in Children: a 29-year Single Center Experience
The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China
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Pseudopubertas Praecox in a 4 Year Old Boy with Bilateral Atypical Adrenocortical Adenomas
Department of General Paediatrics, Adolescent Medicine and Neonatology, Medical Centre, Freiburg, Germany
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