Аутосомно-домінантна атрофія зорового нерва, класична форма
ORPHA:98673· ICD-10 H47.2· Autosomal dominant optic atrophy, classic form
Визначення(English summary)
A rare neuro-ophthalmological disease which is one of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss with an onset during the first decade of life, associated with optic disc pallor, visual acuity loss, visual field deficits and color vision defects.
- Поширеність
- 1-9 / 100 000
- Успадкування
- Autosomal dominant
- Вік початку
- Adolescent, Adult, Childhood