Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep1080 | Late Breaking | ECE2023

Gitelman syndrome, a rare disease: case report

Dumitru Teodora , Preda Cristina , Rosu Andreea , Akad Nada , Anisia Miruna , Leustean Letitia , Christina Ungureanu Maria

Introduction: Gitelman syndrome(GS) is a salt-wasting tubulopathy characterized by renal potassium wasting, hypokalemia, metabolic alkalosis, hypomagnesemia, hypocalciuria and hyperreninemic hyperaldosteronism. It is caused by the mutation of genes encoding sodium chloride (NCCT) and magnesium transporters in the thiazide-sensitive segments of the distal nephron (SLC12A3 and TRMP6 gene). GS is a rare autosomal recessive disease with a prevalence of only 25 cases per one millio...

ea0090ep1142 | Late Breaking | ECE2023

The underneaths of the pituitary stalk

Christina Ungureanu Maria , Preda Cristina , Akad Nada , Dumitru Teodora , Karolina-Agatha Drozdek

We are presenting a 23-year-old girl with a medical history of juvenile rheumatoid polyarthritis treated with methotrexate, that first addressed to the Endocrinology Department in may 2022 for primary amenorrhoea with poorly developed secondary sexual characters: height 160 cm, weight 48 kg, BMI 18.35 kg/m2, Tanner stages P1, B3. She was treated with oral contraceptives by the gynaecologist in the past without a hormonal assessment. The lab work revealed hypogonadotropic hypog...