Inflammatory myopathy in oculopharyngeal dystrophy

E. Peter Bosch, James D.C. Gowans, Theodore Munsat

Research output: Contribution to journalArticle

17 Scopus citations

Abstract

A 75‐year‐old French‐Canadian woman with familial oculopharyngeal dystrophy demonstrated histopathologic alterations similar to those of idiopathic polymyositis. A second biopsy obtained 15 months later was more consistent with previously reported cases. It is suggested that certain patients with oculopharyngeal dystrophy may pass through an initial phase of secondary muscle inflammation similar to that seen in some other heritable myopathies.

Original languageEnglish (US)
Pages (from-to)73-77
Number of pages5
JournalMuscle & Nerve
Volume2
Issue number1
DOIs
StatePublished - Jan 1 1979

ASJC Scopus subject areas

  • Physiology
  • Clinical Neurology
  • Cellular and Molecular Neuroscience
  • Physiology (medical)

Fingerprint Dive into the research topics of 'Inflammatory myopathy in oculopharyngeal dystrophy'. Together they form a unique fingerprint.

  • Cite this

    Bosch, E. P., Gowans, J. D. C., & Munsat, T. (1979). Inflammatory myopathy in oculopharyngeal dystrophy. Muscle & Nerve, 2(1), 73-77. https://doi.org/10.1002/mus.880020111