About Ichthyosis hystrix of Curth-Macklin
Ichthyosis hystrix of Curth-Macklin is a rare disease catalogued by Orphanet (ORPHA:79503). It is associated with the KRT1 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 Ichthyosis hystrix of Curth-Macklin trials.
Search ClinicalTrials.gov for "Ichthyosis hystrix of Curth-Macklin" or filter by Orphanet code ORPHA:79503 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 Ichthyosis hystrix of Curth-Macklin trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Ichthyosis hystrix of Curth-Macklin. Updated daily.