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Xanthopsia is a color vision deficiency in which there is a dominantly yellow bias in vision due to a yellowing of the optical media of the eye. The most common causes are digoxin's inhibitory action on the sodium pump, and the development of cataracts which can cause a yellow filtering effect.
Cyanopsia is a rare visual phenomenon characterized by a blue tint to vision. Most commonly associated with cataract surgery and certain medications, such as sildenafil, cyanopsia is typically a temporary side effect rather than a standalone disease.
Dichromacy, when one of the cones is non-functional and one of the red-green or blue-yellow opponent channels are fully disabled. Cone monochromacy, when two of the cones are non-functional and both chromatic opponent channels are disabled. Vision is reduced to blacks, whites, and greys.
Rarer genetic conditions causing color blindness include congenital blue–yellow color blindness (tritan type), blue cone monochromacy, and achromatopsia. Color blindness can also result from physical or chemical damage to the eye, the optic nerve, parts of the brain, or from medication toxicity. [2] Color vision also naturally degrades in old ...
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 100,000, but is not sex-linked, so affects females and males at similar rates. They tend to confuse greens and blues, and yellow can appear pink.
The four pigments in a bird's cone cells (in this example, estrildid finches) extend the range of color vision into the ultraviolet. [1]Tetrachromacy (from Greek tetra, meaning "four" and chroma, meaning "color") is the condition of possessing four independent channels for conveying color information, or possessing four types of cone cell in the eye.
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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.