小儿肝豆状核变性又称 wilson 氏病,由先天性铜代谢异常引起:系常染色体隐性遗传性疾病。如早期诊断,及时治疗,大多数病人可有正常寿命。因此,儿童期诊断至关重要。但是儿童期本病临床表现多种多样,诊断十分困难。我科近年来共收治该病23例,现将其中误诊且资料完整的12例作一分析。 Wilson’s disease, also known as Wilson’s disease, caused by congenital abnormalities of copper metabolism: Department of autosomal recessive genetic disease. As early diagnosis, timely treatment, most patients have normal life expectancy. Therefore, childhood diagnosis is of paramount importance. However, a variety of clinical manifestations of childhood disease, diagnosis is very difficult. In recent years, our department received a total of 23 cases of the disease, which is now misdiagnosed and 12 cases of complete data for an analysis.