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Eichsfeld type congenital muscular dystrophy

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Description

Desmin-related myopathies (DRM) are a clinically and genetically heterogeneous group of muscular disorders defined morphologically by intrasarcoplasmic aggregates of desmin (DES; 125660), usually accompanied by other protein aggregates. Approximately one-third of DRM are caused by mutations in the desmin gene (Ferreiro et al., 2004). For other forms of DRM, see primary desminopathy (601419).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

182

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Genes

External Links

  • OMIM

    602771

  • Orphanet
  • HPO
  • Medgen

    C0410180

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