Ophthalmic genetics
Branch retinal vein occlusion as a manifestation of systemic vasculopathy in CADASIL: a multimodal imaging case report.
Figen Bezci Aygun, Ceren Özkorkmaz, Sibel Kadayıfcılar
Published: 202510.1080/13816810.2025.2573846
Abstract
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary small vessel disease caused by mutations in the NOTCH3 gene. While it predominantly affects cerebral arterioles, emerging…
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