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  2. Congenital red–green color blindness - Wikipedia

    en.wikipedia.org/wiki/Congenital_red–green...

    The third gene array shows a deuteranopia genotype; the fourth shows a normal color vision genotype. When unequal recombination happens with breaks between the genes (depicted by blue lines), a gene can be essentially deleted from one of the chromosomes. This gene deletion leads to protanopia or deuteranopia (congenital red–green dichromacy).

  3. Usher syndrome - Wikipedia

    en.wikipedia.org/wiki/Usher_syndrome

    The genes also play a role in the development and stability of the retina by influencing the structure and function of both the rod photoreceptor cells and supporting cells called the retinal pigmented epithelium. Mutations that affect the normal function of these genes can result in retinitis pigmentosa and resultant vision loss. [citation needed]

  4. Color blindness - Wikipedia

    en.wikipedia.org/wiki/Color_blindness

    The most common form is caused by a genetic condition called congenital red–green color blindness (including protan and deutan types), which affects up to 1 in 12 males (8%) and 1 in 200 females (0.5%). [3] The condition is more prevalent in males, because the opsin genes responsible are located on the X chromosome. [2]

  5. Pleiotropy - Wikipedia

    en.wikipedia.org/wiki/Pleiotropy

    Pleiotropy can have an effect on the evolutionary rate of genes and allele frequencies. Traditionally, models of pleiotropy have predicted that evolutionary rate of genes is related negatively with pleiotropy – as the number of traits of an organism increases, the evolutionary rates of genes in the organism's population decrease. [10]

  6. Congenital blindness - Wikipedia

    en.wikipedia.org/wiki/Congenital_blindness

    The procedure is a single injection of the AAV2-hRPE65v2 therapeutic gene into the unilateral subretinal of the eye. [39] People must meet the following requirements to be eligible for Luxturna gene therapy: biallelic disease-causing RPE65 mutation, older than one year in age, no surgical contraindications, detectable photoreceptors and RPE ...

  7. Leber's hereditary optic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Leber's_hereditary_optic...

    Leber's hereditary optic neuropathy (LHON) is a mitochondrially inherited (transmitted from mother to offspring) degeneration of retinal ganglion cells (RGCs) and their axons that leads to an acute or subacute loss of central vision; it predominantly affects adult males, and onset is more likely in younger adults.

  8. What your eye color says about you

    www.aol.com/lifestyle/2014-06-10-what-your-eye...

    The reason boils down to genes. A senior lecturer in biomolecular sciences at Liverpool John Moores University said, "What we know now is that eye color is based on 12 to 13 individual variations ...

  9. Retinitis pigmentosa - Wikipedia

    en.wikipedia.org/wiki/Retinitis_pigmentosa

    Visual acuity and color vision can become compromised due to accompanying loss of the cone photoreceptor cells, which are responsible for color vision, visual acuity, and sight in the central visual field. [5] The progression of disease occurs in both eyes in a similar but not identical pattern.