肝豆状核变性是铜代谢障碍所致的一种遗传病,属常染色体隐性遗传。本病多发生于10～25岁,症状多变,常易误诊为肝炎,现报告2例如下。例1,男,7岁半,汉族,河南人,因肝功能异常4年余,加重2月,于1981年6月住传染科。患者出生 Wilson’s disease is a genetic disorder caused by copper metabolism disorder, autosomal recessive inheritance. The disease occurred in 10 to 25 years old, the symptoms varied, often misdiagnosed as hepatitis, are reported in 2 cases as follows. Example 1, male, 7 years and a half, Han, Henan, due to liver dysfunction for more than 4 years, increased in February, in June 1981 lived in infectious diseases. Patient was born