| Literature DB >> 2260849 |
N Sunohara1, K Arahata, E P Hoffman, H Yamada, J Nishimiya, E Arikawa, M Kaido, I Nonaka, H Sugita.
Abstract
We examined dystrophin, the protein product of the Duchenne muscular dystrophy gene, in muscle biopsy specimens from 4 male patients with quadriceps myopathy, all of whom showed a mild and slowly progressive myopathy confined to the quadriceps muscles. All 4 patients had clear abnormalities of dystrophin, and were diagnosed as having Becker muscular dystrophy by both immunofluorescence and immunoblot examinations; that is, dystrophin of an abnormal molecular mass was visualized in muscle cryosections as "patchy" or discontinuous immunostaining at the surface membrane of the muscle fibers. One patient had a brother who showed widespread myopathic changes consistent with typical Becker muscular dystrophy. We conclude that the syndrome called quadriceps myopathy includes a group of forme fruste Becker muscular dystrophy.Entities:
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Year: 1990 PMID: 2260849 DOI: 10.1002/ana.410280506
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422