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Results 1 - 10 of 12 for Cone dystrophy
  1. CNGB3 gene 
    ... in a small percentage of cases of progressive cone dystrophy. Like achromatopsia (described above), this condition affects the ... cones in the retina. However, unlike achromatopsia, progressive cone dystrophy is associated with cones that work normally at ...
    https://medlineplus.gov/genetics/gene/cngb3 - Genetics
  2. CNGA3 gene 
    ... in a small percentage of cases of progressive cone dystrophy. Like achromatopsia (described above), this condition affects the ... cones in the retina. However, unlike achromatopsia, progressive cone dystrophy is associated with cones that work normally at ...
    https://medlineplus.gov/genetics/gene/cnga3 - Genetics
  3. RPGR gene 
    ... disorders. These include cone-rod dystrophy (described above), cone dystrophy, and atrophic macular degeneration. These retinal disorders are ... Mutations in the RPGR gene cause X-linked cone dystrophy. Hum Mol Genet. 2002 Mar 1;11(5): ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  4. GUCY2D gene 
    ... identified in people with a vision disorder called cone-rod dystrophy. The problems associated with this condition include a ... problems worsen over time.The variants that cause cone-rod dystrophy occur in one of the two copies of ...
    https://medlineplus.gov/genetics/gene/gucy2d - Genetics
  5. ABCA4 gene 
    ... been found to cause a vision disorder called cone-rod dystrophy. The problems associated with this condition include a ... for 30 to 60 percent of cases of cone-rod dystrophy that are inherited in an autosomal recessive pattern, ...
    https://medlineplus.gov/genetics/gene/abca4 - Genetics
  6. CRX gene 
    ... the CRX gene have been found to cause cone-rod dystrophy. The problems associated with this condition include a ... color vision. These vision problems worsen over time. Cone-rod dystrophy is caused by mutations that occur in one ...
    https://medlineplus.gov/genetics/gene/crx - Genetics
  7. CACNA1F gene 
    ... This Health Condition MedlinePlus Genetics provides information about Cone-rod dystrophy More About This Health Condition Mutations in the ... These include Åland Island eye disease, X-linked cone-rod dystrophy, an X-linked retinal disorder in New Zealand, ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  8. GNAT2 gene 
    ... Mollon JD, Maher ER, Hunt DM, Moore AT. Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2). Br J Ophthalmol. 2003 Nov; ...
    https://medlineplus.gov/genetics/gene/gnat2 - Genetics
  9. OPN1SW gene 
    ... Neitz M. Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency. J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1438-47. doi: 10.1364/josaa.24.001438. ... of S-opsin causes S-cone-function abnormalities. Vision Res. 2012 Nov 15;73: ...
    https://medlineplus.gov/genetics/gene/opn1sw - Genetics
  10. PRPH2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Cone-rod dystrophy More About This Health Condition Mutations in the ... Holder GE, Bradshaw K, Hunt DM, Moore AT. Cone-rod dystrophy, intrafamilial variability, and incomplete penetrance associated with the ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
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