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Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.
Tateyama, M; Aoki, M; Nishino, I; Hayashi, Y K; Sekiguchi, S; Shiga, Y; Takahashi, T; Onodera, Y; Haginoya, K; Kobayashi, K; Iinuma, K; Nonaka, I; Arahata, K; Itoyama, Y; Itoyoma, Y.
Afiliação
  • Tateyama M; Department of Neurology, Tohoku University School of Medicine, Sendai, Japan. mtateyama@neurol.med.tohoku.ac.jp
Neurology ; 58(2): 323-5, 2002 Jan 22.
Article em En | MEDLINE | ID: mdl-11805270
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.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caveolinas / Distrofias Musculares Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: Neurology Ano de publicação: 2002 Tipo de documento: Article País de afiliação: Japão
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caveolinas / Distrofias Musculares Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: Neurology Ano de publicação: 2002 Tipo de documento: Article País de afiliação: Japão