[A case of mitochondrial myopathy in a family with oculo-pharyngeal myopathy]

Rev Neurol (Paris). 1991;147(6-7):536-7.
[Article in French]

Abstract

We report the case of a patient with mitochondrial lesions, an old woman belonging by her father and mother to a big family with oculopharyngeal muscular dystrophy. Four patients of this family have typical intranuclear tubulo-filamentous inclusions.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Child
  • Female
  • Humans
  • Male
  • Mitochondria, Muscle / pathology*
  • Muscular Diseases / genetics*
  • Muscular Diseases / pathology
  • Ophthalmoplegia / complications
  • Ophthalmoplegia / genetics*
  • Ophthalmoplegia / pathology
  • Pedigree
  • Pharyngeal Diseases / complications
  • Pharyngeal Diseases / genetics*
  • Pharyngeal Diseases / pathology