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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Detalles Bibliográficos
Autores principales: Petraglia, Anthony L., Chengazi, Harris U., Chung, Mina M., Silberstein, Howard J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279990/
https://www.ncbi.nlm.nih.gov/pubmed/22347674
http://dx.doi.org/10.4103/2152-7806.92165

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279990/
https://www.ncbi.nlm.nih.gov/pubmed/22347674
http://dx.doi.org/10.4103/2152-7806.92165

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