... 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 ...

... 20 to 30 percent of all cases of autosomal dominant retinitis pigmentosa, which is thought to be the most common form of the disorder. Rarely, mutations in the RHO gene cause autosomal recessive retinitis pigmentosa. However, this form of the ...

... Condition Mutations in the PRPH2 gene can cause autosomal dominant retinitis pigmentosa, an eye disease that first disrupts night vision ...

... 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 ...

... lack of myosin VIIA in the retina causes retinitis pigmentosa, a condition in which light-sensing cells of the retina gradually ... PubMed ...

... 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 ...

... This Health Condition MedlinePlus Genetics provides information about Retinitis pigmentosa More About This Health Condition BEST1 gene mutations ... individuals with eye abnormalities similar to those in retinitis pigmentosa, although some doctors think these individuals have a ...