About X-linked scapuloperoneal muscular dystrophy
X-linked scapuloperoneal muscular dystrophy is a rare disease catalogued by Orphanet (ORPHA:431272). It is associated with the FHL1 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 X-linked scapuloperoneal muscular dystrophy trials.
Search ClinicalTrials.gov for "X-linked scapuloperoneal muscular dystrophy" or filter by Orphanet code ORPHA:431272 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 X-linked scapuloperoneal muscular dystrophy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked scapuloperoneal muscular dystrophy. Updated daily.