About Mirror-image polydactyly
Mirror-image polydactyly is a rare disease catalogued by Orphanet (ORPHA:498494). It is associated with the PITX1 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 Mirror-image polydactyly trials.
Search ClinicalTrials.gov for "Mirror-image polydactyly" or filter by Orphanet code ORPHA:498494 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 Mirror-image polydactyly trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Mirror-image polydactyly. Updated daily.