Methods：128 patients with Wilson's disease from Jan,1983 to Apr,2000 of our hospital were reviewed.
方法：回顾1983-01/2000-04我院128例肝豆状核变性患者的情况，分析比较患者的临床特点、诊断方法和误诊情况等。
参考来源 - 肝豆状核变性误诊研究 Misdiagnosis of Wilson's DiseaseWilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism. Early diagnosis is important since it can be effectively treated if diagnosis can be made in early life.
肝豆状核变性是一种以铜代谢障碍为特征的常染色体隐性遗传病，早期干预有效，因此早期诊断对疾病的预后有重要意义。
参考来源 - 串联重复ASO探针的构建及其在肝豆状核变性诊断中的应用·2,447,543篇论文数据，部分数据来源于NoteExpress
以上来源于: WordNet
Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.
小结节型肝硬化也可见于Wilson病、原发性胆汁硬化和血色素沉着症。
Hemolytic anemias and psychic aberrations can be the presenting symptoms of Wilson's disease (Chapters 154 and 224).
溶血性贫血和精神异常可出现在Wilson氏病的表现中(第154和224章)。
Objective To summarize experience of selection of donors of living related liver transplantation (LRLT) for Wilson's Disease.
目的总结亲属活体供肝移植治疗肝豆状核变性时选择供者的经验。
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