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
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Case Reports
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English Abstract
MeSH terms
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Child
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Female
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Humans
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Male
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Mitochondria, Muscle / pathology*
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Muscular Diseases / genetics*
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Muscular Diseases / pathology
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Ophthalmoplegia / complications
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Ophthalmoplegia / genetics*
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Ophthalmoplegia / pathology
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Pedigree
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Pharyngeal Diseases / complications
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Pharyngeal Diseases / genetics*
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Pharyngeal Diseases / pathology