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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 the specialized tissue at the back of the eye that detects light and ...
- ... 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 ...
- ... feature. These conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, ...
- ... mental retardation 35 Genetic Testing Registry: Congenital stationary night blindness 1G National Organization for Rare Disorders (NORD) ClinicalTrials. ...
- ... visual acuity) and difficulty seeing in dim light (night blindness). They usually lose areas of vision (visual field ...
- ... experiencing nearsightedness (myopia), difficulty seeing in low light (night blindness), and loss of side (peripheral) vision. Over time, ...
- ... Affected individuals may also experience nearsightedness (myopia), progressive night blindness, or a narrowing of their field of vision. ...
- ... progressive vision problems, including impaired color vision or night blindness. An eye abnormality called a cherry-red spot, ...