Liddle综合征是一种常染色体显性遗传疾病,临床表现酷似原发性醛固酮增多症,故又称为遗传性假性醛固酮增多症。国内报道甚少,现将我科收治的1例报告如下。病例资料患者男,40岁,因间歇性两下肢无力、麻木、行走困难伴高血压5年,加重半年,于1991年9月25日入院。患者在1984年10月因头 Liddle syndrome is an autosomal dominant genetic disease, clinical manifestations resemble primary aldosteronism, it is also known as hereditary aldosteronism. There are few reports in our country. One case reported by our department is reported below. Case data Male, 40 years old, due to intermittent weakness of the lower extremities, numbness, difficulty walking with hypertension for 5 years, increased six months, admitted to hospital on September 25, 1991. Patient in October 1984 due to head