hrp0089p3-p020 | Adrenals and HPA Axis P3 | ESPE2018
Keskin Mehmet
, Koklu Esat
, Kaplan Emel H Aytac
, Karaoglan Murat
, Karaer Kadri
, Keskin Ozlem
Objective: Familial glucocorticoid deficiency (ACTH resistance); is a rare chronic adrenal insufficiency problem. Genetic tranmission is autosomal recessive. Glucocorticoid deficiency is characterized by increased ACTH levels and normal or partial incomplete aldosterone production. The familial glucocorticoid deficiency, which is a defect in the melanocortin receptor. Hypoglycemia, convulsions, increased pigmentation in the skin can be seen from the earliest stages of life.</p...