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远端型重症肌无力

Distal myasthenia gravis.

作者信息

Nations S P, Wolfe G I, Amato A A, Jackson C E, Bryan W W, Barohn R J

机构信息

Department of Neurology, University of Texas Southwestern Medical School, Dallas 75235-8897, USA.

出版信息

Neurology. 1999 Feb;52(3):632-4. doi: 10.1212/wnl.52.3.632.

Abstract

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.

摘要

重症肌无力(MG)的典型表现为累及眼部、延髓及近端肢体肌肉。远端肢体肌肉通常不受累或受累程度较轻。作者对两所大学附属医院神经肌肉诊所治疗的MG患者进行了一项回顾性病历审查。在总共236例患者中,9例(3%)在患病期间远端肢体无力超过近端无力至少一个医学研究委员会分级。手部肌肉,尤其是指伸肌,比远端腿部和足部肌肉更常受累。

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