Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep127 | Bone & Osteoporosis | ECE2016

State of bone mineral density in children with Turner Syndrome in Ukraine

Zelinska Nataliya , Shevchenko Iryna , Globa Evgenia

Background: Low bone mineral density (BMD) and osteoporosis are the frequent consequences of Turner Syndrome (TS).Objective and hypotheses: We examined the BMD in TS girls with different age and karyotype.Methods: Measurements of BMD (g/cm2), Z-score (S.D.) were conducted in 26 girls using X-ray absorptiometry (DEXA) at the lumbar spine L2–L4 depending on the child’s age.<p class="ab...

ea0041ep128 | Bone &amp; Osteoporosis | ECE2016

Osteocalcin as a marker of bone metabolism disorders in girl with Turner syndrome

Zelinska Nataliya , Shevchenko Iryna , Globa Evgenia

Background: One of the markers of bone metabolism is osteocalcin (OC) and Its elevated level indicates osteoporosis.Objective and hypotheses: We investigated the OC level in 14 girls with TS (45,X (n=8), 45,X/46,XX (n=3), structural abnormalities of chromosome X (n=3): seven patients at 4–11 year and 7 – at 12–18 year.Method: DEXA (Z-score, S.D.), serum levels of OC,...

ea0094p261 | Reproductive Endocrinology | SFEBES2023

Gonadectomy in people with a difference of sex development: Initial data from an I-DSD registry prospective quality improvement study

Lucas-Herald Angela , Bryce Jillian , H Davies Justin , Shnorhavorian Margarett , Demir Korcan , de Vries Liat , Elsfedy Heba , Globa Evgenia , Grinspon Romina , Guerra-Junior Gil , Janus Dominika , Faisal Ahmed S , O'Connell Michele

Introduction: There is some variation in the practice of gonadectomy for individuals with Differences of Sex Development (DSD) worldwide. This quality improvement project aims to undertake continued surveillance of the occurrence of gonadectomy in suspected or confirmed cases of DSD.Methods: Participating centres from the International-DSD Registry are sent a monthly email asking if a gonadectomy has been performed. A se...

ea0094op3.1 | Reproductive Endocrinology | SFEBES2023

Are we giving enough attention to blood pressure control in turner syndrome? : Data from the international turner syndrome (I-TS) registry

Mathara Diddhenipothage Shani A.D. , Beck Katharina J. , Amiyangoda C G K , Bryce Jillian , Cima Luminita , De Groote Katya , Deyanova Yana , Globa Evgenia , Herrmann Gloria , Juul Anders , Sophie L. Kjaer Kjaer Anna , Tonnes Pedersen Anette , Poyrazoglu Sukran , Probst-Scheidegger Ursina , Sas Theo C.J. , Fica Simona , Nimali Seneviratne Sumudu , Karolina Witczak Justyna , Orchard Elizabeth , Tomlinson Jeremy W. , Faisal Ahmed S. , Turner Helen E

Introduction: Cardiovascular disease is the commonest cause of death (absolute-excess-risk:41%) in Turner Syndrome (TS). Hypertension is a major risk for circulatory-disease (up to 60%) and a key modifiable-risk factor of aortopathy, ischemic heart disease and stroke in TS. There is no current consensus for hypertension diagnosis/management in TS.Methods: Retrospective multi-centre observational study of patients aged &#...

ea0090oc5.2 | Oral Communications 5: Adrenal and Cardiovascular Endocrinology 1 | ECE2023

The association between hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia

Schroder Mariska , Neacşu Mihaela , Sweep Fred , Span Paul N , Adriaansen Bas , van Herwaarden Antonius , Bryce Jillian , Ahmed Faisal , Ali Salma , Aparecida Sartori Sanchez Bachega Tania , Baronio Federico , Holtum Birkebaek Niels , Bonfig Walter , Clemente Maria , Cools Martine , de Bruin Christiaan , de Vries Liat , Elsedfy Heba , Globa Evgenia , Guran Tulay , Guven Ayla , Amr Nermine Hussein , Januś Dominika , Konrad Daniel , Markosyan Renata , Miranda Mirela , Poyrazoğlu Şukran , Rees Aled , Salerno Mariacarolina , Stancampiano Marianna Rita , Vieitis Ana , Abali Zehra Yavas , - van der Grinten Hedi Claahsen

Background: Testicular Adrenal Rest Tumors (TART) in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD) or 11-hydroxylase deficiency (11OHD) are benign lesions causing testicular damage and infertility. We hypothesize that high ACTH exposure due to poor hormonal control during early life is promoting development of TART later in life.Objective: This study aims to examine the relation between early CAH diagnosis and cons...