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先天性肌无力综合征

Congenital Myasthenic Syndromes.

作者信息

Shieh Perry B, Oh Shin J

机构信息

Department of Neurology, University of California, Los Angeles, 300 Medical Plaza, Suite B-200, Los Angeles, CA 90095, USA.

Department of Neurology, University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL 35233, USA.

出版信息

Neurol Clin. 2018 May;36(2):367-378. doi: 10.1016/j.ncl.2018.01.007.

Abstract

The congenital myasthenic syndromes (CMS) are a group of rare genetic conditions characterized by abnormal neuromuscular transmission. Typically, these conditions have been the result of a dysfunctional protein that is present in the presynaptic terminal, the synaptic cleft, or the postsynaptic terminal. Many of these syndromes present within the first few years of life with fluctuating and fatiguable weakness in a distribution similar to myasthenia gravis, although a limb-girdle distribution and late onset are also seen in certain specific types of CMS. Electrodiagnostic testing with repetitive nerve stimulation may be helpful in some forms of CMS.

摘要

先天性肌无力综合征(CMS)是一组罕见的遗传性疾病,其特征为神经肌肉传递异常。通常,这些疾病是由存在于突触前终末、突触间隙或突触后终末的功能失调蛋白所致。这些综合征中的许多在生命的最初几年内出现,表现为与重症肌无力相似分布的波动性和易疲劳性肌无力,尽管在某些特定类型的CMS中也可见肢带分布和晚发情况。重复神经刺激的电诊断测试可能对某些形式的CMS有帮助。

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