Explore: Retinitis

degeneration (rhodopsin mutation) Retinitis pigmentosa GTPase regulator Retinitis Pigmentosa International "Facts About Retinitis Pigmentosa". National Eye Institute

eye's "sensing" tissue. Retinitis may be caused by a number of different infectious agents. Its most common form, called retinitis pigmentosa, has a prevalence

Usher syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome

Cytomegalovirus retinitis, also known as CMV retinitis, is an inflammation of the retina of the eye that can lead to blindness. Caused by human cytomegalovirus

more sensitive. Defects in the rhodopsin gene cause eye diseases such as retinitis pigmentosa and congenital stationary night blindness. Rhodopsin was discovered

and retinitis pigmentosa is a condition related to changes in mitochondrial DNA. Mutations in the MT-ATP6 gene cause neuropathy, ataxia, and retinitis pigmentosa

rhodopsin gene (RHO), the gene encoding for retinitis pigmentosa GTPase regulator (RGPR), and the gene encoding retinitis pigmentosa 2 protein (RP2). Allelic

those who suffer from retinitis pigmentosa and other degenerative eye diseases, and to find a cure for those diseases. Retinitis pigmentosa Macular degeneration

approved by the U.S. FDA in August 1998, as a treatment for cytomegalovirus retinitis. Several morpholino oligos have been approved to treat specific groups

divided into neoplastic and non-neoplastic conditions. Non-neoplastic: retinitis pigmentosa intraocular foreign body juvenile xanthogranuloma retinal detachment