About Keratoderma hereditarium mutilans with ichthyosis
Keratoderma hereditarium mutilans with ichthyosis is a rare disease catalogued by Orphanet (ORPHA:79395). It is associated with the LORICRIN 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 Keratoderma hereditarium mutilans with ichthyosis trials.
Search ClinicalTrials.gov for "Keratoderma hereditarium mutilans with ichthyosis" or filter by Orphanet code ORPHA:79395 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 Keratoderma hereditarium mutilans with ichthyosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Keratoderma hereditarium mutilans with ichthyosis. Updated daily.