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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.
2023-08-06
KATERYNA KON/Science Photo Library RF/East News
Science Photo Library RF
KATERYNA KON
f0378622
2,13MB
42cm x 42cm przy 300dpi
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,