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Results 1 - 10 of 47 for Nyctalopia
  1. Autosomal recessive congenital stationary 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 ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  2. Autosomal dominant congenital stationary night blindness 
    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 ...
    https://medlineplus.gov/...ant-congenital-stationary-night-blindness - Genetics
  3. X-linked congenital stationary night blindness 
    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 ...
    https://medlineplus.gov/...ked-congenital-stationary-night-blindness - Genetics
  4. Vision - night blindness 
    Night blindness is poor vision at night or in dim light. ... Night blindness may cause problems with driving at night. People with night blindness often have trouble seeing stars ...
    https://medlineplus.gov/ency/article/003039.htm - Medical Encyclopedia
  5. Retinitis pigmentosa 
    Retinitis pigmentosa is an eye disease in which there is damage to the retina . The retina is the layer of tissue at the back of the ...
    https://medlineplus.gov/ency/article/001029.htm - Medical Encyclopedia
  6. Fundus albipunctatus 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/fundus-albipunctatus - Genetics
  7. 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
  8. 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
  9. Vitamin A 
    ... xerophthalmia (unable to see in low light) and night blindness. Vitamin A is in a class of medications ...
    https://medlineplus.gov/druginfo/meds/a621028.html - Drugs and Supplements
  10. 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
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