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肌张力障碍相关基因及临床特征 被引量：3

Genetics and clinical features of dystonia
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摘要 肌张力障碍是由主动肌和拮抗肌的不协调收缩或过度收缩引起的以异常姿势和动作为特征的常见运动障碍性疾病,发病机制复杂,临床表现多样。文章着重论述原发性肌张力障碍、肌张力障碍叠加综合征和遗传性肌张力障碍的致病基因、临床特征及遗传学研究进展。 Dystonia is a common movement disorder characterized by abnormal gestures and involuntary movement as a result of incoordinate contraction of agonistic and antagonistic muscles. The underlying pathogenesis is very complicated and there are various clinical manifestations. The recent findings in genetics and clinical features of primary dystonia, dystoniaplus syndrome and heredodegenerative dystonia are introduced in this paper.
作者 张晓洁 陈晟 乐卫东
机构地区 上海交通大学医学院瑞金医院神经内科
出处 《上海交通大学学报（医学版）》 CAS CSCD 北大核心 2008年第7期908-911,共4页 Journal of Shanghai Jiao tong University:Medical Science
关键词 肌张力障碍 基因 临床特征 dystonia gene clinical features
分类号 R746 [医药卫生—神经病学与精神病学]
  • 相关文献

参考文献32

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共引文献16

同被引文献35

  • 1许晓峰,张晓斌,沙维伟,周朝昀.多巴胺受体与5-羟色胺2A受体基因多态性与迟发性运动障碍的关联[J].中国临床康复,2006,10(34):106-108. 被引量：3
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引证文献3

二级引证文献9

上海交通大学学报（医学版）
2008年 第7期

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