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肝豆状核变性(Wilson 病)是一种常染色体隐性遗传性铜代谢障碍性疾病。临床对早期病例的诊断并不容易。我院近10年以以来共对20例不同肝病患者的肝穿活检组织用电子显微镜观察了肝超微结构改变,发现4例早期肝豆状核变性
Wilson’s disease (Wilson’s disease) is an autosomal recessive inherited disorder of copper metabolism. Clinical diagnosis of early cases is not easy. Nearly 10 years in our hospital a total of 20 cases of liver disease in patients with liver biopsy by electron microscopy of liver ultrastructure changes found in 4 cases of early Wilson’s disease