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Myosin storage myopathy

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Description

Myosin storage myopathy, also known as hyaline body myopathy, is a congenital myopathy characterized by the accumulation of ATPase and antibody positive myosin in hyaline subsarcolemmal bodies in type I muscle fibers. The clinical features are variable, with different patients displaying proximal, scapuloperoneal, or generalized weakness and progressive or nonprogressive courses (summary by Dye et al., 2006).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

166

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Genes

External Links

  • OMIM

    608358

  • Orphanet
  • HPO
  • Medgen

    C1842160

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