A genetic ocular nerve disease marked by optic nerve degeneration. It presents in children between the age of six and twelve years. The condition causes loss of color vision, paracentral /centrocecal field defect and disc atrophy. The visual acuity and severity can range from standard view to legal blindness.
Also Known As
- DOA
- Autosomal Dominant Optic Atrophy
- ADOA
