肝豆状核核变性,又称威尔逊(Wilson)氏病,是一种常染色体隐性遣传的铜代谢障碍疾病,最常侵犯儿童和青年人。本病的临床表现呈多样性,确诊之前易误诊为其他疾病。本科收容1例肝豆状核变性病人,入院前在地方及本院曾误诊为“肾炎”“肝硬化”,入院后肝功能检查有明显损害,肝炎早期肝硬变,为吸取教训,提高对少见病的识别能力,现报告如下: Wilson’s disease, also known as Wilson’s disease, is an autosomal recessive dislocation of copper metabolism that most frequently invades children and young adults. The clinical manifestations of the disease was diversified, easily misdiagnosed as other diseases before diagnosis. Undergraduate admitted to a case of Wilson’s disease patients, before admission in the hospital and hospital have misdiagnosed as “nephritis” “cirrhosis”, liver function tests after admission obvious damage, early liver cirrhosis, to learn lessons to improve the The ability to recognize rare diseases is reported as follows: