Tritanopia

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Tritanopia

Tritanopia (pronounced: tri-ta-no-pee-uh) is a rare, inherited form of color blindness that affects the ability to distinguish between shades of blue and yellow. The term is derived from the Greek words "tritos" (meaning third) and "anopia" (meaning blindness), referring to the third color receptor in the eye being non-functional.

Causes

Tritanopia is caused by a mutation in the SLC6A5 gene, which is responsible for the production of a protein that plays a crucial role in the function of the eye's blue color receptors. This mutation results in the absence of blue color receptors, leading to the characteristic symptoms of Tritanopia.

Symptoms

Individuals with Tritanopia typically have difficulty distinguishing between shades of blue and yellow. They may also have difficulty distinguishing between shades of green and red, although this is less common. Other symptoms may include reduced visual acuity and sensitivity to light.

Diagnosis

Diagnosis of Tritanopia is typically made through a series of color vision tests, such as the Ishihara test or the Farnsworth-Munsell 100 hue test. These tests can help to determine the type and severity of color blindness.

Treatment

There is currently no cure for Tritanopia. However, there are various aids available to help individuals manage their symptoms, such as color-correcting glasses or lenses. Additionally, certain software and apps can adjust the color settings on digital devices to make them easier for individuals with color blindness to use.

See also

References

External links

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