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混合型肝豆状核变性1例报告 被引量:1

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摘要 肝豆状核变性(hepatolenticular degeneration,HLD)又称为Wilson病(Wilson’s disease,WD),是一种常染色体单基因隐性遗传的铜代谢障碍性疾病,由于编码铜跨膜转运蛋白的基因ATP7B发生突变,以致铜在肝脏、大脑及其他组织器官中过度沉积。多数HLD患者以肝病和神经精神症状起病,常累及多个器官,最初的症状往往不易与其他神经系统疾病相鉴别,易误诊[1]。
出处 《中风与神经疾病杂志》 CAS 2021年第2期163-164,共2页 Journal of Apoplexy and Nervous Diseases
关键词 肝豆状核变性 临床表现 诊断 Hepatolenticular degeneration Clinical manifestation Diagnosis
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