Due to the absence of adrenal cortex, the condition causes extreme symptoms of adrenal insufficiency at birth due to very low levels of aldosterone and cortisol. The adrenal medulla can be normally present, poorly formed, or absent, however even so the effects of circulatory catecholamine deficiency are generally mild (due to sympathetic nervous system compensation), except in episodes of hypoglycemia.[2]
Genetics
SF-1 plays a role in the development of adrenal gland. Single gene polymorphism involving SF-1 gene may have a role in adrenal gland agenesis.[1] Various other factors have also been identified.[3][4][5][6]
Diagnosis
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Treatment
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^Else, Tobias; Hammer, Gary Douglas (December 2005). "Genetic analysis of adrenal absence: agenesis and aplasia". Trends in Endocrinology and Metabolism. 16 (10): 458–468. doi:10.1016/j.tem.2005.10.004. PMID16275119. S2CID32644554.