... RHO gene are the most common cause of autosomal dominant retinitis pigmentosa, accounting for 20 to 30 percent of all ... sufficient to cause the disorder. Most people with autosomal dominant retinitis pigmentosa have an affected parent and other family members ...

... include nearsightedness as a feature. These conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch ...

... of rod-cone dystrophy is a condition called retinitis pigmentosa. ABCA4 CACNA1F CNGA3 ... TULP1 UNC119 Cone-rod dystrophy is usually inherited in an autosomal recessive pattern, which means both copies of the ...

... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3( ...

... the eyes (blue sclerae). They may also have retinitis pigmentosa, in which breakdown of the light-sensitive layer ( ... syndrome. COG4 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...