肝豆状核变性是一种遗传性铜代谢异常的疾病,其特点是铜沉积在肝、脑、肾、角膜等组织,由此引起一系列临床症状。现将我院近十年收治的8例肝豆状核变性临床诊治报告如下。临床资料一、发病年龄、性别:8例中男5例,女3例,年龄8～12岁。二、确诊时间:10天1例,14天1例,20天2例, Hepatolenticular degeneration is a hereditary disorder of the metabolism of copper, which is characterized by copper deposition in the liver, brain, kidney, cornea and other tissues, which led to a series of clinical symptoms. Now my hospital admitted to the past decade 8 cases of Wilson’s disease clinical diagnosis and treatment report is as follows. Clinical data First, the age of onset, gender: 8 cases of 5 males and 3 females, aged 8 to 12 years. Second, the diagnosis time: 10 days in 1 case, 14 days in 1 case, 20 days in 2 cases,