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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2012
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| Matèries: | |
| Accés en línia: | 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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