Pigmentary Retinal Dystrophy

Overview of Pigmentary Retinal Dystrophy

Most recent studies have shown that Pigmentary Retinal Dystrophy shares some biological mechanisms with age-related-macular-degeneration, atrophy, blind-vision, congenital-night-blindness, congenital-stationary-night-blindness, disorder-of-eye, dystrophy, eye-diseases-hereditary, hemeralopia, macule, myopia, night-blindness, retinal-degeneration, retinal-diseases, retinal-dystrophies, retinitis-pigmentosa, stargardts-disease, vitamin-a-deficiency.

Among the many pathways, these few ones have gauged particular interests from scientists studying Pigmentary Retinal Dystrophy, and have been seen in publications frequently: Aging, Cardiac Conduction, Cell Death, Excretion, Light Absorption, Localization, Pathogenesis, Phagocytosis, Pigmentation, Regeneration, Transport

Quite a number of genes have been found to play important roles in Pigmentary Retinal Dystrophy, such as ADH7, ERG, FANCA, FANCF, FXN, GRK1, KCNH2, LRAT, RDH12, RDH5, RHO, RLBP1, RPE, RPE65, TNFSF14, TTR. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Pigmentary Retinal Dystrophy Related Genes

click to see detail information for each gene

Pathways Related to Pigmentary Retinal Dystrophy

This information is being compiled and will come in a future update

Related Diseases