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caption

Illustration of a fluorescein angiography view of a retina with hyperfluorescent lesions, windows defects and leakage of lipofuscin in a case of autosomal dominant vitreoretinochoroidopathy, a rare genetic disorder.

headline SPL RF Aug 2023

created date 2023-08-06

credit KATERYNA KON/Science Photo Library RF/East News

source Science Photo Library RF

byline KATERYNA KON

original transmission reference f0378622

weight 2,13MB

size 42cm x 42cm by 300dpi

keywords - Show

1, ABNORMAL, ABNORMALITIES, ARTWORK, ATROPHY, AUTOSOMAL, BEST, bestrophin, bestrophinopathy, CUP, DIAGNOSIS, DIAGNOSTIC, DISC, DISEASE, DISK, DISORDER, DOMINANT, DYSTROPHY, EPITHELIUM, EYE, FOVEA, FUNDOSCOPIC, FUNDOSCOPY, FUNDUS, GENE, GENETIC, HEREDITARY, HYPERPIGMENTATION, ILLUSTRATION, INVESTIGATION, KATERYNA, KON, LIPOFUSCIN, LOSS, MACULA, MACULAR, MEDICAL, MEDICINE, NO-ONE, NOBODY, OCULAR, OPHTHALMOLOGY, OPHTHALMOSCOPY, OPTIC, ORGAN, PERIPHERAL, PIGMENT, PROGRESSIVE, RARE, RETINA, RETINAL, RETINOSCHISIS, RETINOSCOPY, UNHEALTHY, VESSEL, VISION, vitreoretinochoroidopathy, VITREOUS,