重症肌无力
医学
弱点
手部肌肉
肌肉无力
神经肌肉接头
物理医学与康复
物理疗法
外科
解剖
心理学
内科学
神经科学
作者
Sharon Nations,Gil I. Wolfe,Anthony A. Amato,Carlayne E. Jackson,Wilson W. Bryan,Richard J. Barohn
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:1999-02-01
卷期号:52 (3): 632-632
被引量:69
摘要
Myasthenia gravis (MG) characteristically involves ocular, bulbar, and proximal extremity muscles. Distal extremity muscles are typically spared or less prominently involved. The authors performed a retrospective chart review of MG patients treated at two university-based neuromuscular clinics. From a total population of 236, nine patients (3%) had distal extremity weakness exceeding proximal weakness by at least one Medical Research Council grade during their illness. Hand muscles, particularly finger extensors, were involved more frequently than were distal leg and foot muscles.
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