About Dubowitz syndrome
Dubowitz syndrome is a rare disease catalogued by Orphanet (ORPHA:235). It is associated with the LIG4, NSUN2 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 Dubowitz syndrome trials.
Search ClinicalTrials.gov for "Dubowitz syndrome" or filter by Orphanet code ORPHA:235 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 Dubowitz syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Dubowitz syndrome. Updated daily.