![]() ![]() Color blindness can also result from physical or chemical damage to the eye, the optic nerve, or parts of the brain. ![]() Females who are not color-blind can carry genes for color blindness and pass them on to their children. Males are more likely to be color blind than females, because the genes responsible for the most common forms of color blindness are on the X chromosome. ![]() The most common form is caused by a genetic disorder called congenital red–green color blindness. The most common cause of color blindness is an inherited problem or variation in the functionality of one or more of the three classes of cone cells in the retina, which mediate color vision. People with total color blindness (achromatopsia) may also be uncomfortable in bright environments and have decreased visual acuity. However, issues are generally minor, and people with colorblindness automatically develop adaptations and coping mechanisms. Color blindness may make some academic activities more difficult. It can impair tasks such as selecting ripe fruit, choosing clothing, and reading traffic lights. Red–green: 8% males, 0.5% females (Northern European descent) Ĭolor blindness or color vision deficiency ( CVD) is the decreased ability to see color or differences in color. Genetic ( inherited usually X-linked) Īdjustments to teaching methods, mobile apps Viewers with normal color vision should clearly see the number "74". Color vision deficiency, impaired color vision Įxample of an Ishihara color test plate. ![]()
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