Clinical-histopathological correlation in a case of Coats' disease

BACKGROUND: Coats' disease is a non-hereditary ocular disease, with no systemic manifestation, first described by Coats in 1908. It occurs more commonly in children and has a clear male predominance. Most patients present clinically with unilateral decreased vision, strabismus or leukocoria. Th...

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Detalles Bibliográficos
Autores principales: Fernandes, Bruno F, Odashiro, Alexandre N, Maloney, Shawn, Zajdenweber, Moyses E, Lopes, Andressa G, Burnier, Miguel N
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564043/
https://www.ncbi.nlm.nih.gov/pubmed/16942617
http://dx.doi.org/10.1186/1746-1596-1-24

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564043/
https://www.ncbi.nlm.nih.gov/pubmed/16942617
http://dx.doi.org/10.1186/1746-1596-1-24

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