Gene: [0X^/NYS1] nystagmus 1, congenital; [NYS ]
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SUM |
Congenital nystagmus is an idiopathic disorder characterized by bilateral ocular oscillations usually manifest during infancy. Vision is typically decreased due to slippage of images across the fovea. As such, visual acuity correlates with nystagmus intensity, which is the amplitude and frequency of eye movements at a given position of gaze. X-linked, autosomal dominant, and autosomal recessive pedigrees have been described, see GEM:06p12/NYS2; GEM:00.0/NYS3." |
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REF |
PHE,FOG "Berry AC, Docherty Z: Am J Med Genet, 43, 896, 1992 PHE,FOG "Billings: J Hered, 33, 457, 1942 PHE,FOG "Gutmann DH &: Am J Med Genet, 43, 897, 1992 PHE,FOG "Gutmann DH &: Am J Med Genet, 39, 167-169, 1991 HET "Kerrison JB &: Genomics, 33, 523-526, 1996 PHE,FOG "Rucker: AJHG, 1, 52-54, 1949 PHE,FOG "Waardenburg &: (in) Genetics & Ophthalmol, Oxford, Blackwell, 1961 |
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KEY |
neu, eye |
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CLA |
unknown, basic |
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LOC |
0X |
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MIM |
MIM: 310700 |
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SYN |
NYS |
