Abstract
3 Beta-Hydroxysteroid Dehydrogenase (3B-HSD) deficiency is a rare form of Congenital Adrenal Hyperplasia (CAH). It is an autosomal recessive disease leading to varying degrees of enzymatic defects. Presented is a case of late onset type 2 3B-HSD deficiency, diagnosed as a work up of infertility, adrenal adenoma, and high dehydroepiandrosterone sulfate (DHEA-S) levels.
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