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- W2116714417 abstract "Sturge-Weber syndrome (SWS) is a sporadic congenital neurooculocutaneous disorder that may present with glaucoma and vascular malformations of the conjunctiva, episclera, choroid and retina. We report a case of localized choroidal haemangioma associated with SWS Type I. A 26-year-old male with a port-wine stain birthmark on right side of the face was admitted to our clinic with complaints of photophobia, pain, and blurred vision in his right eye. Anterior segment examination of the right eye revealed dilatation and tortuosity of conjunctival vessels. Snellen visual acuity was 0.4 (20/50) and intraocular pressure - normal. Fluorescein angiography demonstrated a smallspotted hyperfluorescent mass nasal to the optic disc and exudative retinal detachment in the central zone. Testing of the left eye found no abnormalities. Brain CT scans showed bilateral tram-track calcifications. This case report arouses certain clinical interest because of its rare incidence, continued asymptomatic development, and delayed diagnosis only after the presentation of exudative retinal detachment with subsequent visual deficit. Neuroophthalmological monitoring of patients with SWS may be useful for early detection of ocular involvement before the appearance of serious visual complications." @default.
- W2116714417 created "2016-06-24" @default.
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- W2116714417 date "2008-01-01" @default.
- W2116714417 modified "2023-09-27" @default.
- W2116714417 title "LOCALIZED CHOROIDAL HAEMANGIOMA ASSOCIATED WITH STURGE - WEBER SYNDROME: A CASE REPORT" @default.
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