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以共济失调为首发症状、急性起病的肝豆状核变性1例报告
作者: 陈蕾 周东 徐严明
单位:四川大学华西医院神经内科,成都,610041
关键词: 肝豆状核变性 共济失调 遗传
分类号:
出版年·卷·期(页码):2009·35·第 1 期(0-0)
摘要:
肝豆状核变性(hepatolenticuhr degeneration,HLD)又称Wil-son's病,是一种常染色体隐性遗传性铜代谢障碍性疾病,锥体外系症状和体征是最常见的神经系统损害表现,且多隐匿起病,首发临床症状多样,缺乏特异性,给本病的早期诊断带来一定困难.
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