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Congenital Stationary Night "Blindness," Dominant
- Autosomal dominant congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
- ... RHO gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by a loss of vision ... over time. Unlike retinitis pigmentosa (described below), autosomal dominant congenital stationary night blindness does not affect daytime vision.The RHO gene ...
- ... GNAT1 gene have been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindness. Hum Mutat. 2007 Jul;28(7):741-2. ...
- ... 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 gene in autosomal dominant stationary ... to congenital stationary night blindness impairs the enzyme inhibition by ...
- Vision Impairment and Blindness (National Library of Medicine)What is vision impairment? Vision impairment is the loss of vision. It includes blindness, which means that you have lost all or most of your sight. It ...
- ... 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. ...
- ... as a feature. These conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, ...
