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- W2006692638 abstract "Idiopathic retinal vasculitis, aneurysms and neuroretinitis (IRVAN) syndrome is a rare but well recognized clinical entity. It is characterized by bilateral disease with retinal vasculitis, aneurysmal dilatations of arterioles, exudation in retina and neuroretinitis. Chang et al first recognized this new entity and proposed the acronym IRVAN.1 Since then various reports of IRVAN syndrome have appeared in literature. Samuel et al conducted largest cohort study and gave detailed observation and proposed staging of this syndrome.2 The disease characteristically involves young individuals who have no associated systemic illness.1–3 Involvement is typically bilateral with exudation in macula causing vision impairment. Peripheral capillary non perfusion is another feature of this entity and predisposing factor for vision loss.1,3We report a case of a young male patient with bilateral vision loss and typical features of IRVAN syndrome who was managed successfully at our centre." @default.
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- W2006692638 date "2015-07-01" @default.
- W2006692638 modified "2023-10-17" @default.
- W2006692638 title "A rare case of idiopathic retinal vasculitis, aneurysms and neuroretinitis (IRVAN) syndrome" @default.
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- W2006692638 doi "https://doi.org/10.1016/j.mjafi.2014.07.011" @default.
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