Heterochromia and ocular ischemia resulting from Neurofibromatosis I-related optic pathway glioma

Abstract

NF1-OPG are typically benign optic nerve tumors arising in childhood which may be associated with visual loss from optic neuropathy, impaired extraocular motility, and proptosis. While optic disc edema, pallor, or choroidal folds are commonly observed, iris and retinal vascular sequelae arising from NF1-OPG are exceedingly rare (1-4)

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