现将我科1980～1987年收治的7例先天性肾上腺皮质增生报告如下。临床资料一、分型及临床表现本组21-羟化酶缺陷6例,17-羟化酶缺陷1例。前者6例全皆男性。<3月2例,1～4岁3例,5岁1例。入院时均有频繁呕吐、腹泻、脱水,并伴有皮肤色泽加深。其中1例出现呼吸困难、紫绀,另1例出现抽搐,均有阴囊及阴茎增大。17-羟化酶缺陷型的患儿为12岁女性,呈进行性 Now my department from 1980 to 1987 admitted 7 cases of congenital adrenal hyperplasia report as follows. Clinical data First, the classification and clinical manifestations The group of 21-hydroxylase deficiency in 6 cases, 17-hydroxylase deficiency in 1 case. The former 6 cases were all men. <2 cases in March, 1 to 4 years in 3 cases, 1 case of 5 years old. Frequent admission vomiting, diarrhea, dehydration, and accompanied by deepened skin color. One case of dyspnea, cyanosis, another case of convulsions, scrotum and penis have increased. 17-hydroxylase-deficient children were 12-year-old women, was progressive