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