About Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy is a rare disease catalogued by Orphanet (ORPHA:329336). It is associated with the RRM2B, RNASEH1 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy trials.
Search ClinicalTrials.gov for "Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy" or filter by Orphanet code ORPHA:329336 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy. Updated daily.