１３例２１羟化酶缺乏症的诊断与治疗向承发，任丽，夏礼勤，唐瑟２１羟化酶缺乏症是肾上腺皮质激素先天合成缺陷中最常见的一种，属常染体隐性遗传［１，５］。男女表现各异，现将收治的１３例报告如下。１临床资料１．１一般资料男８例、女５例，年龄７天～１４岁。１．... 13 cases of 21 hydroxylase deficiency diagnosis and treatment Xiang Cheng, Ren Li, Xia Liqin, Tang Se 21 hydroxylase deficiency is adherent cortical hormone congenital synthesis defects in the most common one, is an autosomal recessive [1,5]. The performance of men and women vary, now admitted to the 13 cases are as follows. 1 Clinical data 1.1 General Information 8 males and 5 females, aged 7 days to 14 years. 1. ...