摘要
家族性淀粉样多发性神经病(familial amyloid polyneuropathy,FAP)是一种主要以常染色体显性遗传为特征的多发性神经病,其发病年龄、临床表现有许多不同的报道。现悉本病主要由转甲状腺素蛋白(TTR)、apoAl、gelsolin三种蛋白质的变异所致,但是其表型和基因型的关系仍不明了。肝脏移植是目前有效的治疗方式,且需在早期进行。
出处
《国外医学（神经病学．神经外科学分册）》
2003年第2期122-125,共4页
Foreign Medical Sciences（Section On Neurology & Neurosurgery）
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