ea0093oc13 | Oral communication 2: Neuroendocrinology | EYES2023
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 ...