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Leber congenital amaurosis associated with Chiari I malformation: Two cases and a review of the literature

OBJECTIVE: Leber congenital amaurosis (LCA) is a rare, clinically and genetically heterogeneous disorder characterized by severe loss of vision in the first year of life, affecting approximately 3000 people in the United States. Some LCA patients manifest developmental abnormalities of the central n...

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Main Authors: Petraglia, Anthony L., Chengazi, Harris U., Chung, Mina M., Silberstein, Howard J.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Medknow Publications & Media Pvt Ltd 2012
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3279990/
https://ncbi.nlm.nih.gov/pubmed/22347674
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2152-7806.92165
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