About Autosomal recessive isolated optic atrophy
Autosomal recessive isolated optic atrophy is a rare disease catalogued by Orphanet (ORPHA:98676). It is associated with the YME1L1, MECR, ACO2 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 Autosomal recessive isolated optic atrophy trials.
Search ClinicalTrials.gov for "Autosomal recessive isolated optic atrophy" or filter by Orphanet code ORPHA:98676 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 Autosomal recessive isolated optic atrophy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Autosomal recessive isolated optic atrophy. Updated daily.