This is an observational study of patients with Primary Mitochondrial Disease with either signs or symptoms suggestive of myopathy. The Investigator will identify potential patients through existing medical records and one on-site visit.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Assess the relationship of genotype to phenotype in patients with Primary Mitochondrial Disease
Timeframe: 1 year
Compare local and regional differences in standard of care and management of patients with Primary Mitochondrial Disease
Timeframe: 1 year