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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Limb-girdle muscular dystrophy, type 2C


Other Names for this Disease
  • Adhalin deficiency, secondary
  • DMDA
  • DMDA1
  • Duchenne-like muscular dystrophy, autosomal recessive, type 1
  • Epileptic encephalopathy with global cerebral demyelination
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Tests & Diagnosis

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Testing

  • Orphanet lists international laboratories offering diagnostic testing for this condition.
Other Names for this Disease
  • Adhalin deficiency, secondary
  • DMDA
  • DMDA1
  • Duchenne-like muscular dystrophy, autosomal recessive, type 1
  • Epileptic encephalopathy with global cerebral demyelination
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.