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Congenital stationary night "blindness," autosomal dominant 3
- ... NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2 NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3 NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; ...
- ... the RHO gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by a loss of vision ... stationary) over time. Unlike retinitis pigmentosa (described below), ... stationary night blindness does not affect daytime vision.The RHO gene ...
- ... the GNAT1 gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... active mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindness. Hum Mutat. 2007 Jul;28(7):741-2. ...
- ... the PDE6B gene has been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... rod cGMP-phosphodiesterase beta-subunit rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta ... missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness. Nat Genet. 1994 May;7(1):64-8. ...
- ... no history of the disorder in their family. Autosomal dominant mental retardation 35 Genetic Testing Registry: Congenital stationary night blindness 1G National Organization for Rare Disorders (NORD) ClinicalTrials. ...
- ... include nearsightedness as a feature. These conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, ...
