About Congenital multicore myopathy with external ophthalmoplegia
Congenital multicore myopathy with external ophthalmoplegia is a rare disease catalogued by Orphanet (ORPHA:98905). It is associated with the RYR1 gene. 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 Congenital multicore myopathy with external ophthalmoplegia trials.
Search ClinicalTrials.gov for "Congenital multicore myopathy with external ophthalmoplegia" or filter by Orphanet code ORPHA:98905 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 Congenital multicore myopathy with external ophthalmoplegia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital multicore myopathy with external ophthalmoplegia. Updated daily.