Ophtalmological Pathology and Management in Eye Diseases: Retina Distrophies and Degenerations
摘要
Retinal distrophy at the nivel of the rods, retinitis- retinitis pigmentoza- is a hereditary group of diffuse idiopathic familiar, progressive retinal dystrophies wich be accompanied by posterior subcapsular cataract, open angle glaucoma, myopia, keratoconus, intermediate uveitis. RP is presents in syndromes. Retinal dystrophies at the level of the cones are: Startgardt disease, fundus flavimaculatus, progressive con/dystrophies, Bests’ disease. Choroidal dystrophies are choroideremie, gyrate athrophie. Vitroretinal dystrophies are: retinoschizis congenital, Goldman Favre. Vitreoretinal degenerations are: Wagner Jansen, Stickler syndrome. Peripheric retinal degenerations may be lattice degeneration, degenerative retinoschizis.