About Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Skin fragility-woolly hair-palmoplantar keratoderma syndrome is a rare disease catalogued by Orphanet (ORPHA:293165). It is associated with the DSP 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 Skin fragility-woolly hair-palmoplantar keratoderma syndrome trials.
Search ClinicalTrials.gov for "Skin fragility-woolly hair-palmoplantar keratoderma syndrome" or filter by Orphanet code ORPHA:293165 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 Skin fragility-woolly hair-palmoplantar keratoderma syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Skin fragility-woolly hair-palmoplantar keratoderma syndrome. Updated daily.