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Diseases

Genetic and Rare Diseases Information Center (GARD)

X-linked myopathy with excessive autophagy


Other Names for this Disease
  • XMEA
  • Myopathy, X-linked, with excessive autophagy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Research

Clinical Trials & Research for this Disease

  • The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.
  • The U.S. National Institutes of Health, through the National Library of Medicine, developed ClinicalTrials.gov to provide patients, family members, and members of the public with current information on clinical research studies. There is a study titled Study of Inherited Neurological Disorders which may be of interest to you. To find this trial, click on the link above.
  • Orphanet lists European clinical trials, research studies, and patient registries enrolling people with this condition. 
Other Names for this Disease
  • XMEA
  • Myopathy, X-linked, with excessive autophagy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.