| Literature DB >> 1944407 |
R Pauzner1, I Blatt, M Mouallem, E Ben-David, Z Farfel, M Sadeh.
Abstract
A family with oculopharyngeal muscular dystrophy (OPMD) is described. Histological and histochemical studies of muscle biopsy showed nonspecific myopathic changes; no "ragged-red" fibers were seen. Electron microscopy demonstrated bizarre large mitochondria with abnormal cristae, but no intranuclear inclusion bodies. Our findings are compatible with the possibility that OPMD is a heterogeneous syndrome, and may be a manifestation of mitochondrial myopathy.Entities:
Mesh:
Year: 1991 PMID: 1944407 DOI: 10.1002/mus.880141004
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217