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连枷臂综合征临床特点分析
引用本文:陈清兰,丁冬雪,冯燕燕,张晨,田发发.连枷臂综合征临床特点分析[J].国际神经病学神经外科学杂志,2016,43(1):27-29.
作者姓名:陈清兰  丁冬雪  冯燕燕  张晨  田发发
作者单位:中南大学湘雅医院神经内科,湖南省长沙市,410008
摘    要:连枷臂综合征是肌萎缩侧索硬化的一种良性的临床变异型,一般男性多见,起病缓慢,生存期较长,主要临床特征为对称性双上肢近端显著的肌无力、肌萎缩,而双下肢、球部功能受累较轻。神经电生理检查表现为3个以上脊髓节段的广泛神经源性损害。目前缺乏针对连枷臂综合征的药物研究,利鲁唑是唯一批准用于肌萎缩侧索硬化的药物。

关 键 词:肌萎缩侧索硬化  连枷臂综合征
收稿时间:2015/12/6 0:00:00
修稿时间:2016/2/13 0:00:00

Clinical features of flail arm syndrome
CHEN Qing-Lan,DING Dong-Xue,FENG Yan-Yan,ZHANG Chen,TIAN Fa-Fa.Clinical features of flail arm syndrome[J].Journal of International Neurology and Neurosurgery,2016,43(1):27-29.
Authors:CHEN Qing-Lan  DING Dong-Xue  FENG Yan-Yan  ZHANG Chen  TIAN Fa-Fa
Institution:Department of Neurology, Xiangya Hospital of Central South University, Changsha 410008, China
Abstract:Flail arm syndrome (FAS) is a benign clinical variant of amyotrophic lateral sclerosis (ALS). It occurs predominantly in males and has a slow onset and a long survival. The major clinical features of FAS are significant muscle weakness and amyotrophia in the proximal segments of both upper limbs and mild involvement of both lower limbs and bulbar muscles. Nerve electrophysiological examination shows extensive neurogenic damage in more than three segments of the spinal cord. At present, there are no drugs for FAS, and riluzole is the only drug approved for the treatment of ALS.
Keywords:amyotrophic lateral sclerosis  flail arm syndrome
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