肝豆状核变性是一种并不十分罕见的常染色体隐性遗传性疾病。目前已有较为有效的治疗措施,但其临床表现错综复杂,类型不一,因而诊断甚易漏误,特别在小儿更是如此。我院1958—1981年经角膜裂隙灯检查、血清铜蓝蛋白测定及尸解确诊的30例,现简报如下。临床资料一、一般资料本组病例男17例,女13 Wilson’s disease is a rare, autosomal recessive disease. At present there are more effective treatment measures, but the clinical manifestations of complex, different types, which is very easy to diagnose errors, especially in children is even more so. Our hospital 1958-1981 corneal slit lamp examination, serum ceruloplasmin and autopsy confirmed the diagnosis of 30 cases are as follows. Clinical data First, the general information The group of male patients 17 cases, 13 female