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脊髓性肌阵挛临床研究进展
引用本文:林傲,何怡婧,靳令经. 脊髓性肌阵挛临床研究进展[J]. 国际神经病学神经外科学杂志, 2020, 47(3): 338-342
作者姓名:林傲  何怡婧  靳令经
作者单位:同济大学附属同济医院神经内科, 上海 200065
基金项目:上海市卫生系统优秀人才培养计划(2017BR029)
摘    要:脊髓性肌阵挛是一种相对罕见的肌阵挛类型,可由各种原发或继发脊髓病变导致,其表现复杂、鉴别困难、难以治疗。根据起源及传播方式不同,主要分为脊髓固有性肌阵挛及脊髓节段性肌阵挛两种类型,系统比较二者临床表现、病因、发病机制、诊断及治疗等特征将为临床实践提供指导,该文就相关临床研究进展进行综述。

关 键 词:脊髓性肌阵挛|脊髓固有性肌阵挛|脊髓节段性肌阵挛
收稿时间:2020-02-27
修稿时间:2020-05-11

Progress in clinical research on spinal myoclonus
LIN Ao,HE Yi-Jing,JIN Ling-Jing. Progress in clinical research on spinal myoclonus[J]. Journal of International Neurology and Neurosurgery, 2020, 47(3): 338-342
Authors:LIN Ao  HE Yi-Jing  JIN Ling-Jing
Affiliation:Department of Neurology, Tongji Hospital Affiliated to Tongji University, Shanghai 200065, China
Abstract:Spinal myoclonus is a relatively rare type of myoclonus, which can be caused by various primary or secondary spinal cord lesions. It has complex manifestations and is difficult to identify and treat. According to the origin and mode of transmission, it is mainly divided into propriospinal myoclonus and spinal segmental myoclonus. A systematic comparison of the clinical manifestations, etiology, pathogenesis, diagnosis, and treatment between the two will provide guidance for clinical practice. This article reviews the progress in relevant clinical research.
Keywords:spinal myoclonus|propriospinal myoclonus|spinal segmental myoclonus
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