Distal myasthenia gravis

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

Research output: Contribution to journalArticle

47 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)632-634
Number of pages3
JournalNeurology
Volume52
Issue number3
Publication statusPublished - Feb 1999

    Fingerprint

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Nations, S. P., Wolfe, G. I., Amato, A. A., Jackson, C. E., Bryan, W. W., & Barohn, R. J. (1999). Distal myasthenia gravis. Neurology, 52(3), 632-634.