Amaurosis congenita of Leber: A rare genetic eye disorder characterized by blindness at birth or within years as well as other eye abnormalities. More detailed information about the symptoms, causes, and treatments of Amaurosis congenita of Leber is available below.
See full list of 7 symptoms of Amaurosis congenita of Leber
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Amaurosis congenita of Leber as a "rare disease".
Source - Orphanet
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