About Anophthalmia/microphthalmia-esophageal atresia syndrome
Anophthalmia/microphthalmia-esophageal atresia syndrome is a rare disease catalogued by Orphanet (ORPHA:77298). It is associated with the SOX2 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 Anophthalmia/microphthalmia-esophageal atresia syndrome trials.
Search ClinicalTrials.gov for "Anophthalmia/microphthalmia-esophageal atresia syndrome" or filter by Orphanet code ORPHA:77298 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 Anophthalmia/microphthalmia-esophageal atresia syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Anophthalmia/microphthalmia-esophageal atresia syndrome. Updated daily.