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Night blindness
- Autosomal recessive congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
- 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 ...
- X-linked congenital stationary night blindness is a disorder of the retina, which is a specialized tissue at the back of the eye that detects light ... condition typically have difficulty seeing in low light (night blindness). They also have other vision problems, including increased ...
- ... an impaired ability to see in low light (night blindness) and the presence of whitish-yellow flecks in ... an eye examination.Individuals with fundus albipunctatus experience night blindness from an early age. In particular, they have ...
- ... identified in people with X-linked congenital stationary night blindness. NYX gene variants are responsible for the complete ... is characterized by difficulty seeing in low light (night blindness), loss of sharpness (reduced visual acuity), severe nearsightedness ( ...
- ... identified in people with X-linked congenital stationary night blindness. CACNA1F gene variants are responsible for the incomplete ... individuals also have difficulty seeing in low light (night blindness).Variants in the CACNA1F gene change the structure ...
- ... been found to cause autosomal dominant congenital stationary night blindness, which is characterized by a loss of vision ... retinitis pigmentosa (described below), autosomal dominant congenital stationary night blindness does not affect daytime vision.The RHO gene ...
- ... been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... an mGluR6 point mutant associated with congenital stationary night blindness. Mol Pharmacol. 2009 Nov;76(5):992-7. ...
- ... been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... by the brain as not meaningful, resulting in night blindness. More About This Health Condition CSNBAD3 GBT1 GNAT1_ ...
- ... been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... by the brain as not meaningful, resulting in night blindness. More About This Health Condition MedlinePlus Genetics provides ...
