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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
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| Materias: | |
| 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 |