About Rothmund-Thomson syndrome type 3
Rothmund-Thomson syndrome type 3 is a rare disease catalogued by Orphanet (ORPHA:715640). It is associated with the CRIPT 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 Rothmund-Thomson syndrome type 3 trials.
Search ClinicalTrials.gov for "Rothmund-Thomson syndrome type 3" or filter by Orphanet code ORPHA:715640 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 Rothmund-Thomson syndrome type 3 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Rothmund-Thomson syndrome type 3. Updated daily.