先天性肾上腺增生,17-α羟化酶缺乏征甚为罕见。临床主要特点是高血压、低血钾、碱中毒、性幼雅。极易与原发性醛固酮增多征(以下简称原醛)相混淆。本文报告1例并进行分析讨论,以期提高对本征的认识。临床资料患者女,15岁,1989年12入院。主诉发作性四肢乏力,麻痹,伴夜尿7年。患者于 Congenital adrenal hyperplasia, 17-α-hydroxylase deficiency syndrome is rare. The main clinical features are high blood pressure, hypokalemia, alkalosis, sexual elegance. Easily and primary aldosteronism syndrome (hereinafter referred to as the original aldehyde) confused. This article reports 1 case and analyzes the discussion, with a view to raising awareness of the intrinsic. Clinical data Female patient, 15 years old, admitted to hospital in 1989. Main complaints of limb weakness, paralysis, with nocturia for 7 years. Patient at