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Results 1 - 9 of 9 for Nyctalopia
  1. NYX gene 
    ... 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 ( ...
    https://medlineplus.gov/genetics/gene/nyx - Genetics
  2. CACNA1F gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  3. RHO gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  4. GRM6 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. ...
    https://medlineplus.gov/genetics/gene/grm6 - Genetics
  5. GNAT1 gene 
    ... 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_ ...
    https://medlineplus.gov/genetics/gene/gnat1 - Genetics
  6. TRPM1 gene 
    ... been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics
  7. PDE6B gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/pde6b - Genetics
  8. RP2 gene 
    ... retinitis pigmentosa. This condition primarily affects males, causing night blindness in early childhood followed by progressive daytime vision ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  9. RPGR gene 
    ... retinitis pigmentosa. This condition primarily affects males, causing night blindness in early childhood followed by progressive daytime vision ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics