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Amaurosis congenita of Leber

Disease AmaurosisAmaurosis fugax

Amaurosis congenita of Leber- type 2
Overview
A rare inherited retinal disease (retinal dystrophy) that starts during the fetal stage. Vision impairment is obvious at birth or within months of birth.

 


Amaurosis congenita of Leber ... clouding of eye lenses, sensitivity to light, rapid involuntary eye movements, blindness
Amaurosis congenita of Leber, type 1 ... nystagmus, sensitivity to light, impaired vision, blindness ...

See also: Amaurosis, Symptom, Dystrophy, Vision impairment, Injury

Disease AmaurosisAmaurosis fugax

 
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