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非典型２１－羟化酶缺乏症（ＮＣ２１－ＯＨＤ）为先天性肾上腺皮质增生症中２１－羟化酶（Ｐ４５０Ｃ２１）缺乏的一种类型，１９５７年由Ｊａｙｌｅ等首先描述，呈常染色体隐性遗传。因多于青少年围青春期或成人发病，且症状轻微，故又名迟发型或轻型２１－ＯＨＤ。１发...
Atypical 21-hydroxylase deficiency (NC21-OHD) is a type of 21-hydroxylase (P450C21) deficiency in congenital adrenal hyperplasia, first described by Jayle et al in 1957 as autosomal recessive . Due to more than adolescent adolescence or adult onset, and minor symptoms, it is also known as delayed type or light 21-OHD. 1 hair ...