| Literature DB >> 11805270 |
M Tateyama1, M Aoki, I Nishino, Y K Hayashi, S Sekiguchi, Y Shiga, T Takahashi, Y Onodera, K Haginoya, K Kobayashi, K Iinuma, I Nonaka, K Arahata, Y Itoyama, Y Itoyoma.
Abstract
The authors describe a patient with sporadic distal myopathy associated with reduced caveolin-3 in muscle fibers in which the muscle atrophy was restricted to the small muscles of the hands and feet. Gene analysis disclosed a heterozygous 80 G-->A substitution in the caveolin-3 gene that was identical to that of reported cases of elevated serum creatine kinase. This patient further demonstrated possible clinical heterogeneity of myopathies with mutations in the caveolin-3 gene.Entities:
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Year: 2002 PMID: 11805270 DOI: 10.1212/wnl.58.2.323
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910