About Congenital muscular dystrophy with intellectual disability and severe epilepsy
Congenital muscular dystrophy with intellectual disability and severe epilepsy is a rare disease catalogued by Orphanet (ORPHA:329178). It is associated with the DPM2 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 muscular dystrophy with intellectual disability and severe epilepsy trials.
Search ClinicalTrials.gov for "Congenital muscular dystrophy with intellectual disability and severe epilepsy" or filter by Orphanet code ORPHA:329178 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 muscular dystrophy with intellectual disability and severe epilepsy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital muscular dystrophy with intellectual disability and severe epilepsy. Updated daily.