About Hypotrichosis simplex of the scalp
Hypotrichosis simplex of the scalp is a rare disease catalogued by Orphanet (ORPHA:90368). It is associated with the KRT74, CDSN 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 Hypotrichosis simplex of the scalp trials.
Search ClinicalTrials.gov for "Hypotrichosis simplex of the scalp" or filter by Orphanet code ORPHA:90368 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 Hypotrichosis simplex of the scalp trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hypotrichosis simplex of the scalp. Updated daily.