About Marie Unna hereditary hypotrichosis
Marie Unna hereditary hypotrichosis is a rare disease catalogued by Orphanet (ORPHA:444). It is associated with the EPS8L3, HR 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 Marie Unna hereditary hypotrichosis trials.
Search ClinicalTrials.gov for "Marie Unna hereditary hypotrichosis" or filter by Orphanet code ORPHA:444 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 Marie Unna hereditary hypotrichosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Marie Unna hereditary hypotrichosis. Updated daily.