肝豆状核变性又称Wilson氏病,是一种常染色体隐性遗传的铜代谢障碍病。国外统计发病率为1/20万。国内1951～1982年初,共报道本病247例。我院1956年6月～1982年底共有住院病者43例。本文主要从临床角度分析本院的误诊病例,冀能从中吸取教训,提高早期诊断率。临床资料男24例,女19例。发病年龄6～36岁,平均18.5岁,以11～20岁多见(25例,58.1%)。本组病例的基本病征:①肝脏病史或/及肝脏 Wilson’s disease, also known as Wilson’s disease, is an autosomal recessive disorder of copper metabolism. The incidence of foreign statistics 1/20000. Domestic 1951 ~ early 1982, a total of 247 cases reported this disease. Our hospital from June 1956 to the end of 1982 a total of 43 cases of inpatients. This article mainly from the clinical point of view of misdiagnosis cases in our hospital, hoping to learn from them and improve the early diagnosis rate. Clinical data of 24 males and 19 females. The age of onset was 6 to 36 years (average 18.5 years old), and was more common in 11 ~ 20 years (25 cases, 58.1%). The basic symptoms of this group of patients: ① history of liver disease or / and liver