Cargando…
RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3′-end of ORF15
PURPOSE: To describe a group of patients with retinitis pigmentosa GTPase regulator (RPGR)-related retinopathy with a tapetal-like retinal sheen and corresponding changes in the reflectivity of the ellipsoid zone on optical coherence tomography (OCT) imaging. METHODS: A retrospective case series of...
Autores principales: | Benson, Matthew D., Mukherjee, Souvick, Agather, Aime R., Blain, Delphine, Cunningham, Denise, Mays, Robert, Sun, Xun, Li, Tiansen, Hufnagel, Robert B., Brooks, Brian P., Huryn, Laryssa A., Zein, Wadih M., Cukras, Catherine A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501488/ https://www.ncbi.nlm.nih.gov/pubmed/37695603 http://dx.doi.org/10.1167/iovs.64.12.19 |
Ejemplares similares
-
Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies
por: Malechka, Volha V., et al.
Publicado: (2022) -
Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy
por: Pfister, Tyler A., et al.
Publicado: (2021) -
Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort
por: Serpen, Jasmine Y., et al.
Publicado: (2020) -
Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics Imaging
por: Liu, Tao, et al.
Publicado: (2022) -
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome
por: Huryn, Laryssa A, et al.
Publicado: (2023)