Clinical Observation of the Bilateral Retinal Vein Occlusion

The clinical evaluation was done in eighteen eyes of nine patients with bilateral BRVO in aspects of onset, visual acuity, interval between onset of one eye and the other, sex ratio, associated systemic diseases, location of the affected vein, the effect of macular edema on visual acuity and ocular complications. The onset of age was from fifty one to sixty eight years. Eight patients were women, and one patient was man. Hypertension was the most common associated systemic disease. Ten eyes (55.5%) of bilateral BRVO were affected the superior temporal branch vein, the sites of occlusion were not more than two disc diameters from the optic disc in fifteen eyes (83.3%). The complications of seevere visual loss had macular edema, macular capillary nonperfusion, retinal neovascularization and vitreous hemorrhage. Among of six numbers who could be followed up more than one year, and visual acuity of five eyes with macula edema were decreased than five other eyes developed one year or later. Eyes that were more than five disc diameters of capillary nonperfusion, as visualized with fluorescence angiography were thirteen (72.2%). Of these eyes, six (46.1 %) eyes occured retinal neovascularization, five of those had macular capillary nonperfusion. four of those were 0.1 in final vision. Three of four eyes with vitreous hemorrhage were very slowly improved in visual acuity, but another was decreasing in visual acuity due to other ocular complications We thought that woman with history of BRVO due to hypertension in sixth and seventh decades should be followed up the other eye for three years.

Bilateral Juvenile Retinoschisis in four Brothers of a Family

Juvenile retinoschisis is a vitreoretinal dystrophy with X-linked recessive mode of transmission that shows microcystic degeneration of the macula associated with splitting of the sensory retina, predominantly within the nerve fiber layer. We experienced X-linked juvenile retinoschisis, in four borthers within a family in which were the onset of visual disturbance between second decades and third decades, and all showed maculopathy, RPE atrophy, vitreous veils extended to vitreous, partial optic atrophy, specific electroretinographic findings.