About Focal palmoplantar keratoderma with joint keratoses
Focal palmoplantar keratoderma with joint keratoses is a rare disease catalogued by Orphanet (ORPHA:370002). It is associated with the DSG1 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 Focal palmoplantar keratoderma with joint keratoses trials.
Search ClinicalTrials.gov for "Focal palmoplantar keratoderma with joint keratoses" or filter by Orphanet code ORPHA:370002 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 Focal palmoplantar keratoderma with joint keratoses trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Focal palmoplantar keratoderma with joint keratoses. Updated daily.