
Von Hippel Lindan disease is a rare congenital vascular malformation afflicting the retinal and central nervous system blood vessels. A boy aged 12 years suffering from this angiomatosis with bilateral involvement was examined. Fundus both eyes revealed marked vascular malformation in the form of extreme venous dilatation and tortuosity along with angioma formation. There was no associated central nervous system involvement in this case.
Male, Ophthalmology, Angiomatosis, von Hippel-Lindau Disease, Retinal Diseases, Fundus Oculi, Humans, RE1-994, Child
Male, Ophthalmology, Angiomatosis, von Hippel-Lindau Disease, Retinal Diseases, Fundus Oculi, Humans, RE1-994, Child
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