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[肌强直的临床肌电图和神经肌电图特征]

[Clinico-electromyographic and electroneuromyographic characteristics of myotonias].

作者信息

Avakian G N, Aslanov A M, Odilzhonov T O, Antipin E S

出版信息

Zh Nevropatol Psikhiatr Im S S Korsakova. 1986;86(3):335-8.

PMID:3705838
Abstract

Clinical and electrophysiological examinations of 24 patients with myotonia (Thomsen's myotonia--10 patients and myotonic dystrophy--14 patients) ascertained criteria of the general and differential diagnosis of myotonia. Apart from electromyographic changes the patients presented a considerable decrease in the speed of afferent and efferent conduction of impulses along peripheral nerves in myotonic dystrophy, which justifies the inclusion into combined therapy of means improving conduction along nerve fibers.

摘要

对24例肌强直患者(10例汤姆森型肌强直和14例强直性肌营养不良)进行了临床和电生理检查,确定了肌强直的一般诊断标准和鉴别诊断标准。除肌电图改变外,强直性肌营养不良患者沿周围神经的传入和传出冲动传导速度显著降低,这证明在联合治疗中应纳入改善神经纤维传导的方法。

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