The human eye is a truly remarkable and intricately designed system. A healthy eye has millions of retinal photoreceptors in the form of rods and cones, allowing us to translate light into colour. As a result, most of us are able to see at least a million different colours, with some experts maintaining that the true number is as high as high as 10 million.1 This astounding perceptive ability is surpassed by few species in the natural world and suggests that colour vision has conferred important evolutionary benefits for humans, perhaps explaining why we have developed such strong emotional associations with and preferences for certain hues. However, congenital or acquired damage to any component within the delicate optical apparatus can impair your ability to accurately perceive colour and there are a number of inherited disorders, diseases, and medications known to interfere with colour vision.
Inherited Colour Vision Disorders
Most colour vision impairment is the result of inherited colour vision disorders that arise due to abnormal photoreceptor cell function, including:
Red-Green Colour Blindness
Red-green colour blindness is a sex-linked trait and by far the most common colour vision disorder, affecting up to 8% of men and 0.5% of women. This type of colour blindness results from missing or damaged L-cones (protanopia or protanomaly) or missing or damaged M-cones (deuteranopia or deuteranomaly), creating difficulties distinguishing between reds and greens as well as blues and greens, grays and purples.
Blue-Yellow Colour Blindness
Blue-yellow colour blindness is far rarer than red-green colour blindness, representing fewer than 1 in 10,000 people with colour vision disorders, and is not sex-linked, meaning men and women are affected equally.
This condition can either take the form of tritanopia, in which S-cones are completely missing, or tritanomaly, in which S-cones are present but damaged. Blue-yellow colour blindness can be a misleading name, as the disorder does not create difficulties distinguishing between blues and yellows, but rather, causes those with the disorder to confuse yellow with violet and blue with green.
Achromatopsia
Achromatopsia is a hereditary disorder that results from abnormal cone function, significantly reducing or eliminating your ability to see colour. Unlike what is typically called colour blindness, achromatopsia is rare, affecting between 1 in 30,000 and 1 in 50,000 people, and involves a complete or near-complete lack of colour vision; in the most severe cases, you see only shades of white, black and grey.
In addition to impaired colour perception, achromatopsia causes a number of additional vision problems, including involuntary eye movements, low visual acuity and increased light sensitivity.
Cone-Rod Dystrophy
Cone-rod dystrophy is an inherited disease that damages light-sensitive cells in the retina, impairing vision sharpness, peripheral vision, and colour perception in an estimated 1 in 40,000 people. In some cases, colour vision impairment is present at birth. In other cases, photoreceptors deteriorate over time to progressively impede colour perception.
A number of health conditions can damage eye tissue and create colour vision changes. Image Source: Pexels user Tomasz Bazylinski