Congenital and inborn causes of primary adrenal insufficiency
Category and cause | Key featuresa | |
---|---|---|
Congenital adrenal hyperplasia1 | 21-Hydroxylase deficiency | Most common subtype Classic variant causes deficiency of both cortisol and aldosterone Can also cause virilization in females due to accumulation of dehydroepiandrosterone metabolites |
11-Beta-hydroxylase deficiency | Accumulation of aldosterone precursor 11-deoxycorticosterone results in hypertension and hypokalemia | |
3-Beta-hydroxylase deficiency | Lack of dehydroepiandrosterone conversion to testosterone causes ambiguous genitalia in boys | |
Other enzymatic abnormality17 | Aldosterone synthase deficiency | Isolated mineralocorticoid deficiency |
Deficiency of P450 side-chain cleavage enzyme | Slows the rate-limiting step in cortisol synthesis | |
ACTH resistance23 | Familial glucocorticoid deficiency type 1 | Tall stature, isolated deficiency of glucocorticoids, and generally normal aldosterone production |
3A (Allgrove, AAA) syndrome | Achalasia, Addison disease, alacrimia, AAAS gene mutation | |
Adrenoleuko dystrophy23 | Accumulation of very long chain fatty acid in adrenal cortex | Inhibited response to ACTH; X-linked recessive disorder associated with neurologic deficits that predominantly affects males and typically presents in adolescence |
Congenital adrenal dysgenesis1 | Congenital but can also be secondary to ACTH deficiency | Hypotrophy of adrenal cortex, adrenal insufficiency, hypogonadism, especially in males due to reduction in adrenal androgens |
Others (rare)1,17,23 | Wolman disease | Lysosomal acid lipase deficiency that results in accumulation of fat and diffuse punctate adrenal calcification causing adrenal insufficiency Very poor prognosis |
Abetalipoproteinemia | Fat malabsorption results in lack of cholesterol to make steroids | |
Mitochondrial disorders | External ophthalmoplegia, retinal degeneration, cardiac conduction defects |
↵aNot all listed primary adrenal conditions necessarily present with both glucocorticoid and mineralocorticoid deficiency.
AAA = achalasia, Addison disease, alacrimia; ACTH = adrenocorticotropic hormone