TY - JOUR T1 - Choroidal osteoma in association with Stargardt’s dystrophy JF - British Journal of Ophthalmology JO - Br J Ophthalmol SP - 978 LP - 979 DO - 10.1136/bjo.2006.098186 VL - 91 IS - 7 AU - Edwin C Figueira AU - R Max Conway AU - Ian C Francis Y1 - 2007/07/01 UR - http://bjo.bmj.com/content/91/7/978.abstract N2 - Choroidal osteoma usually occurs in 20–30 year old, healthy, white women as a well-defined, unilateral (75%), solitary, yellow orange, slow-growing juxtapapillary lesion.1 This is the first time that a choroidal osteoma has been associated with Stargardt’s dystrophy. A 16-year-old girl presented with bilateral reduction of distance visual acuity (6/24) since 2 years. Near vision, colour vision, stereoacuity and anterior segments of both eyes were normal. Amsler grid testing in the left eye revealed a blur of the grid superotemporal to the foveal fixation point. Stereoscopic funduscopy revealed bilateral Stargardt’s maculopathy (foveolar pigment epithelial changes with parafoveal orange-coloured flecks; figs 1A,B), with an approximately 2.5 mm yellowish subretinal lesion situated 2-disc diameters below the left optic disc (fig 1B). Fundus fluorescein angiography (FFA) revealed macular and perimacular hypofluorescence (dark choroid) with hyperfluorescence and late … ER -