vitreoretinochoroidopathy

navigate by keyword : autosomal dominant vitreoretinochoroidopathy best gene bestrophin bestrophinopathy disk disorder dystrophy epithelium eye fovea fundoscopic fundoscopy fundus genetic hereditary illustration investigation lipofuscin macula macular medical ocular ophthalmologist ophthalmology ophthalmoscopy optic cup organ patient pigment progressive rare disease retina retinal retinoscopy vessel vision loss peripheral retinoschisis vitreous abnormalities atrophy hyperpigmentation

Autosomal dominant vitreoretinochoroidopathy, illustration showing circular band of hyperpigmentation in the retina Royalty Free Stock Photo

Bestrophinopathies, inherited retinal disorders caused by mutations in the BEST1 gene, 3D illustration Royalty Free Stock Photo

Bestrophinopathies, inherited retinal disorders caused by mutations in the BEST1 gene, illustration Royalty Free Stock Photo

Molecular model of Bestrophin-1 protein Best 1, 3D illustration. A protein responsible for regulating calcium signaling Royalty Free Stock Photo

Autosomal dominant vitreoretinochoroidopathy, illustration showing hyperfluorescent lesions and leakage of lipofuscin

Molecular model of Bestrophin-1 protein Best 1, 3D illustration. A protein responsible for regulating calcium signaling in cells Royalty Free Stock Photo

Autosomal dominant vitreoretinochoroidopathy, a rare genetic disorder, an illustration showing hyperfluorescent lesions, windows defects, and leakage of lipofuscin on fluorescein angiogram