About Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome
Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome is a rare disease catalogued by Orphanet (ORPHA:538574). It is associated with the KRT1, MPZ 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 Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome trials.
Search ClinicalTrials.gov for "Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome" or filter by Orphanet code ORPHA:538574 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 Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome. Updated daily.