Current perspectives in Bietti crystalline dystrophy

Bietti crystalline dystrophy (BCD) is a rare-inherited disease caused by mutations in the CYP4V2 gene and characterized by the presence of multiple shimmering yellow-white deposits in the posterior pole of the retina in association with atrophy of the retinal pigment epithelium (RPE) and chorioretin...

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Detalles Bibliográficos
Autores principales: García-García, GP, Martínez-Rubio, M, Moya-Moya, MA, Pérez-Santonja, JJ, Escribano, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679682/
https://www.ncbi.nlm.nih.gov/pubmed/31440027
http://dx.doi.org/10.2147/OPTH.S185744

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679682/
https://www.ncbi.nlm.nih.gov/pubmed/31440027
http://dx.doi.org/10.2147/OPTH.S185744

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