Reticular dystrophy of the retinal pigment epithelium

Reticular dystrophy of the retinal pigment epithelium is a patterned dystrophy of the retinal pigment epithelium, of progressive course, characterized by the presence of a bilateral hyperpigmented reticular pattern resembling a fishnet with knots, resulting in a slowly progressive loss of vision that often only becomes apparent in old age. Reticular dystrophy of the retinal pigment epithelium is sometimes associated with scleral staphyloma, choroidal neovascularization, convergent strabismus, spherophakia with myopia and luxated lenses, and partial atrophy of the iris.

Also known as: reticular dystrophy of retinal pigment epithelium, retinal dystrophy, reticular pigmentary, of POSTERIOR POLE

25 clinical trials for this condition and its sub-types, 0 tagged with Reticular dystrophy of the retinal pigment epithelium itself.