Searchable abstracts of presentations at key conferences in endocrinology

ea0093oc13 | Oral communication 2: Neuroendocrinology | EYES2023

Hypogonadotropic hypogonadism in a patient with Allgrove syndrome: A case report

Gheorghe-Milea Ana , Rusu Eva , Stănoiu-Pinzariu Oana , Georgescu Carmen Emanuela

Background: Triple A (Allgrove) syndrome is a rare genetic disorder with autosomal recessive inheritance, caused by mutations in the AAAS gene on chromosome 12q13. It is characterized by the following triad: ACTH-resistant adrenal insufficiency, alacrimia, and achalasia.Case presentation: We present the case of a 19-year-old male who was diagnosed with adrenal insufficiency at the age of five following an addisonian crisis with hypoglycemic coma. At the ...