Argus II retinal prosthesis system: a review of patient selection criteria, surgical considerations, and post-operative outcomes

Retinitis pigmentosa (RP) is a group of heterogeneous inherited retinal degenerative disorders characterized by progressive rod and cone dysfunction and ensuing photoreceptor loss. Many patients suffer from legal blindness by their 40s or 50s. Artificial vision is considered once patients have lost...

Descripción completa

Detalles Bibliográficos
Autores principales: Finn, Avni P, Grewal, Dilraj S, Vajzovic, Lejla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005308/
https://www.ncbi.nlm.nih.gov/pubmed/29942114
http://dx.doi.org/10.2147/OPTH.S137525

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005308/
https://www.ncbi.nlm.nih.gov/pubmed/29942114
http://dx.doi.org/10.2147/OPTH.S137525

Ejemplares similares