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Congenital 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 ...
- ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
- X-linked congenital stationary night blindness is a disorder of the retina, which is a specialized tissue at the back of the eye that ... typically not affected in people with X-linked congenital stationary night blindness.The vision problems associated with X-linked congenital ...
- ... Amaurosis, Leber congenital Congenital amaurosis of retinal origin Congenital retinal blindness CRB Dysgenesis neuroepithelialis retinae Hereditary epithelial dysplasia of ...
- ... as a feature. These conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, ...
- ... Autosomal dominant mental retardation 35 Genetic Testing Registry: Congenital stationary night blindness 1G National Organization for Rare Disorders (NORD) ClinicalTrials. ...
- ... Norrie disease. Anderson-Warburg syndrome Atrophia bulborum hereditaria Congenital progressive oculo-acoustico-cerebral degeneration Episkopi blindness Fetal iritis syndrome Norrie syndrome Norrie's disease ...
- ... vision problems, including impaired color vision or night blindness. An eye ... congenital, infantile, and juvenile forms. The features of congenital ...
- ... hyperekplexia) to unexpected stimuli. Some affected individuals have blindness due to impairment of the area of the ... for processing vision, called the occipital cortex (cortical blindness).People with asparagine synthetase deficiency typically do not ...
- ... to reduction in side (peripheral) vision and eventual blindness. Other signs and symptoms may include bulging eyes, ... without other associated abnormalities, it is called primary congenital glaucoma.Other individuals experience early onset of primary ...