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  2. Color blindness - Wikipedia

    en.wikipedia.org/wiki/Color_blindness

    The cause of blue–yellow color blindness is not analogous to the cause of red–green color blindness, i.e. the peak sensitivity of the S-opsin does not shift to longer wavelengths. Rather, there are 6 known point mutations of OPN1SW that degrade the performance of the S-cones. [46] The OPN1SW gene is almost invariant in the human population.

  3. Monochromacy - Wikipedia

    en.wikipedia.org/wiki/Monochromacy

    Ophthalmology. Monochromacy (from Greek mono, meaning "one" and chromo, meaning "color") is the ability of organisms to perceive only light intensity without respect to spectral composition. Organisms with monochromacy lack color vision and can only see in shades of grey ranging from black to white. Organisms with monochromacy are called ...

  4. Cerebral achromatopsia - Wikipedia

    en.wikipedia.org/wiki/Cerebral_achromatopsia

    Cerebral achromatopsia. Cerebral achromatopsia is a type of color blindness caused by damage to the cerebral cortex of the brain, rather than abnormalities in the cells of the eye's retina. It is often confused with congenital achromatopsia but underlying physiological deficits of the disorders are completely distinct.

  5. Congenital red–green color blindness - Wikipedia

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

    Frequency. 2-9% males; <1% females. Congenital red–green color blindness is an inherited condition that is the root cause of the majority of cases of color blindness. It has no significant symptoms aside from its minor to moderate effect on color vision. [ 1] It is caused by variation in the functionality of the red and/or green opsin ...

  6. Achromatopsia - Wikipedia

    en.wikipedia.org/wiki/Achromatopsia

    Achromatopsia. Achromatopsia, also known as rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy. Historically, the name referred to monochromacy in general, but now typically refers only to an autosomal recessive congenital color vision condition.

  7. Visual impairment - Wikipedia

    en.wikipedia.org/wiki/Visual_impairment

    Visual impairment. Visual or vision impairment ( VI or VIP) is the partial or total inability of visual perception. In the absence of treatment such as corrective eyewear, assistive devices, and medical treatment, visual impairment may cause the individual difficulties with normal daily tasks, including reading and walking. [ 6]

  8. Dichromacy - Wikipedia

    en.wikipedia.org/wiki/Dichromacy

    Deuteranopia is a severe form of red-green color blindness, in which the M-cone is absent. It is sex-linked and affects about 1% of males. Color vision is very similar to protanopia. [2] Tritanopia is a severe form of blue-yellow color blindness, in which the S-cone is absent. It is much rarer than the other types, occurring in about 1 in ...

  9. Cortical blindness - Wikipedia

    en.wikipedia.org/wiki/Cortical_blindness

    Cortical blindness is the total or partial loss of vision in a normal-appearing eye caused by damage to the brain 's occipital cortex. [ 1] Cortical blindness can be acquired or congenital, and may also be transient in certain instances. [ 2] Acquired cortical blindness is most often caused by loss of blood flow to the occipital cortex from ...

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