Phenotypic Differences in a PRPH2 Mutation in Members of the Same Family Assessed with OCT and OCTA

Choroidal dystrophies comprise a group of chorioretinal degenerations. However, the different findings observed among these patients make it difficult to establish a correct clinical diagnosis. The objective of this study was to characterize new clinical findings by optical coherence tomography (OCT...

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Detalles Bibliográficos
Autores principales: Albertos-Arranz, Henar, Sánchez-Sáez, Xavier, Martínez-Gil, Natalia, Pinilla, Isabel, Coco-Martin, Rosa M., Delgado, Jesús, Cuenca, Nicolás
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146155/
https://www.ncbi.nlm.nih.gov/pubmed/33925984
http://dx.doi.org/10.3390/diagnostics11050777

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8146155/
https://www.ncbi.nlm.nih.gov/pubmed/33925984
http://dx.doi.org/10.3390/diagnostics11050777

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