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. Author manuscript; available in PMC: 2017 Sep 7.
Published in final edited form as: J Investig Med. 2010 Dec;58(8):938–944. doi: 10.231/JIM.0b013e3181ff6bb8

Figure 2.

Figure 2

Normal and abnormal adrenal steroidogenesis in the zona fasciculata. The normal pathway is shown on the left. Loss of function mutations in CYP21A2 (steroid 21-hydroxylase) lead to congenital adrenal hyperplasia (CAH; right), resulting in a massive increase in 17-hydroxyprogesterone. This 17-hydroxyprogesterone and upstream precursors are metabolized to androgens, probably via several distinct pathways.