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Early-onset myopathy with fatal cardiomyopathy

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Description

Salih myopathy is characterized by muscle weakness (manifest during the neonatal period or in early infancy) and delayed motor development; children acquire independent walking between ages 20 months and four years. In the first decade of life, global motor performance is stable or tends to improve. Moderate joint and neck contractures and spinal rigidity may manifest in the first decade but become more obvious in the second decade. Scoliosis develops after age 11 years. Cardiac dysfunction manifests between ages five and 16 years, progresses rapidly, and leads to death between ages eight and 20 years, usually from heart rhythm disturbances.

GeneReviews

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

2,220

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Genes

External Links

  • OMIM

    611705

  • Orphanet

    289377

  • HPO
  • Medgen

    C2673677

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