About Brittle cornea syndrome
Brittle cornea syndrome is a rare disease catalogued by Orphanet (ORPHA:90354). It is associated with the ZNF469, PRDM5 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 Brittle cornea syndrome trials.
Search ClinicalTrials.gov for "Brittle cornea syndrome" or filter by Orphanet code ORPHA:90354 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 Brittle cornea syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Brittle cornea syndrome. Updated daily.