Anti-SRP myopathy

研究成果: Article

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Detection of autoantibodies can provide more important clinical information in assigning patients to clinical subsets, selecting a therapy and predicting prognosis. Muscle biopsy is the principal examination for a diagnosis of myositis; however, autoantibody detection is also useful. Myositis-associated autoantibodies, detected in 30% of myositis patients, can be screened by RNA immunoprecipitation assay. Some case series have revealed that the anti-SRP antibody, detected in 5-8% of polymyositis patients, was generally associated with severe and refractory polymyositis. However, it has been accepted that anti-SRP myopathy should be separated from polymyositis based on histological and clinical features. Some patients with anti-SRP myopathy show chronic progression indistinguishable from muscular dystrophy.

元の言語English
ページ(範囲)961-963
ページ数3
ジャーナルClinical Neurology
51
発行部数11
DOI
出版物ステータスPublished - 2011 12 1

ASJC Scopus subject areas

  • Clinical Neurology

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