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Late-onset isolated ACTH deficiency

MONDO:0016042

Late-onset isolated ACTH deficiency is a rare, acquired, pituitary hormone deficiency characterized by secondary adrenal insufficiency, with normal secretion of anterior pituitary hormones, except for ACTH. Patients present with weakness, fatigue, weight loss, anorexia, vomiting/nausea, hypoglycemia, and abnormally low serum ACTH and cortisol levels. Association with autoimmune disease such as Hashimoto's thyroiditis has been described.

1 clinical trial for this condition and its sub-types, 0 tagged with Late-onset isolated ACTH deficiency itself.

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