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Colour blindness: types, tests and why it mostly affects men

In Europe about 8 men in 100 confuse some colours, against fewer than one woman in 100. What colour blindness is, how it is inherited, how it is detected and what studies say about glasses ‘for the colour-blind’.

By the editorial teamUpdated 9 min read10 studies and sources citedAI-generated text
Illustration The same apple tree seen with all three types of cones and, on the right, simulated with deuteranopia and protanopia: the red of the fruit merges with the green of the leaves.

The condition owes its traditional name, Daltonism, to John Dalton, the English chemist who at the end of the eighteenth century described his own difficulty in distinguishing certain colours. About 150 years after his death, genetic analysis made it possible to establish what his defect really was1. Colour blindness, in the meantime, has turned out to be one of the most common vision disorders3.

The large population surveys indicate that, among people of European origin, it affects about 8 men in 100 and 4 women in 1,0002. It is an enormous difference between the sexes, and the explanation lies in a chromosome.

In brief

  • Congenital colour blindness affects about 8% of men and 0.4% of women of European origin2.
  • The most common form, red-green, is passed on with the X chromosome: this is why it affects mostly males1,3.
  • It is almost never a true blindness to colours: some colours are confused, while the complete loss of colour vision is rare1,4.
  • An alteration of colours can also appear during life because of diseases of the eye, the nervous system or other organs: in this case it must be assessed7.
  • The glasses and coloured filters studied so far change the perception of some shades, but do not restore normal colour vision3,9.
In this article
  1. What colour blindness is
  2. Why colour blindness mostly affects men
  3. Acquired colour blindness
  4. In everyday life
  5. Glasses for the colour-blind: what the studies say
  6. Frequently asked questions
  7. Sources

What colour blindness is

We see colours thanks to the cones, cells of the retina that contain light-sensitive pigments. There are three types, sensitive to long, medium and short wavelengths: simplifying, to reds, greens and blues1,4. The brain compares the signals of the three types and works out the colour from them.

In congenital colour blindness one of these pigments works differently from usual or is missing4. In the first case colours are perceived, but some shades are confused; in the second the range of distinguishable colours is reduced further. The main types are:

TypeCones involvedHow common it is
Protan (red-green)sensitive to long wavelengthstogether with deutan, the great majority of cases4
Deutan (red-green)sensitive to medium wavelengthstogether with protan, the great majority of cases4
Tritan (blue-yellow)sensitive to short wavelengthscongenital, one person in several tens of thousands4
Achromatopsiano functioning conesrare1

The red-green forms are milder than achromatopsia, the rare complete loss of colour vision, which does not depend on the pigment genes but on other cone proteins1,4. In other words, the image of the colour-blind person who sees ‘in black and white’ corresponds only to a very small minority.

Why colour blindness mostly affects men

The genes for the red- and green-sensitive pigments are on the X chromosome, in a row: a red gene followed by one or more green genes. The blue one is instead on chromosome 71. The red and green genes are almost identical, 96%, and this similarity favours recombination errors: a gene can be lost or fuse with the other into a ‘hybrid’ gene. This is the mechanism behind most red-green forms1,5. The retina uses only the first two genes in the row, and how marked the defect is depends, roughly, on how different the pigments they produce are1,5.

Men have only one X chromosome: if it carries an altered gene, the defect shows. Women have two, and almost always the second compensates3. This is why many more women carry the alteration without showing it, the so-called carriers: according to an estimate based on the frequency in men, between 9 and 15%6. A son of a carrier mother can inherit the X chromosome with the altered gene.

The frequency also varies between populations. A review of population surveys found values between 4 and 6.5% in men of Chinese and Japanese origin, lower than in Europe; the review attributes the differences mainly to chance factors in the history of the populations rather than to natural selection2.

Acquired colour blindness

Not all colour alterations are present from birth. Colour vision that changes during life can depend on diseases that affect the transparent structures of the eye, the retina, the optic nerve, up to the visual cortex of the brain, or on general diseases7. In acquired forms an alteration on the blue-yellow axis is more frequent7, so much so that a blue defect suggests first of all an acquired cause, given that the congenital form is so rare4.

Telling a congenital form from an acquired one may require several tests: plate tests, hue-arrangement tests, the anomaloscope and sometimes genetic analysis4. Plates are a simple screening method, but on their own do not give a diagnosis4. How they work and how reliable they are is explained in our article on colour blindness tests.

In everyday life

A 2019 review identified 20 studies on the impact of colour blindness in daily life and grouped them into seven themes: everyday activities, work, choosing products, emotions, school and vocational training, self-care and health, and even some advantages. The most recurrent difficulty concerned work, but the authors stress that the studies are few and concern very specific groups, such as drivers and medical students8.

For congenital forms, management today consists mainly of information and guidance, including in the choice of profession3. Some jobs, in fact, have specific requirements for colour vision.

Glasses for the colour-blind: what the studies say

Glasses and contact lenses with coloured filters are sold, presented as aids for people who confuse colours. The available evidence calls for caution.

The study

Red lenses for red-green colour blindness

In a 1997 randomised trial, people with congenital red-green colour blindness tried for a week glasses with filters that let through mainly red light. The lenses improved results in tests that asked them to tell apart very different colours, such as red from green, but mainly because they changed the apparent brightness of colours; they worsened results in finer tests and with colours on the blue-yellow axis. 56% of participants judged the lenses fairly or very useful, but only 17% intended to get a pair: among the reasons for refusal were colour distortion and the fact of perceiving fewer colours10.

A 2022 systematic review pooled 16 studies of different types, including comparisons between groups, prototypes, single cases and narrative reviews, on electronic and optical devices for colour blindness, including commercially available glasses and contact lenses. The conclusions: there is no evidence of a clinically relevant improvement in colour perception, although some shades may be perceived differently9. A review from 2010 already observed that these aids can help in specific tasks, but do not allow normal colour discrimination to be reached3. For the future, the same review indicated gene therapy as a possibility, on the basis of results in animals3; where research stands for inherited retinal diseases is described in our article on gene therapy.

When to talk to an ophthalmologist

  • If you notice that colours look different from before, for example duller: an acquired alteration can be a sign of a disease of the eye or of the nervous system7.
  • If a child often confuses colours: a test can clear up the doubt, and knowing also helps in choices of study and work3. When the vision of the youngest is checked is explained in our article on a child’s first eye examination.
  • Before enrolling in a course of study or a job with colour vision requirements3,8.
  • If you are considering glasses or filters ‘for the colour-blind’: talk to the ophthalmologist to know what to expect, in the light of the studies9,10.

Frequently asked questions

Can colour blindness be cured?

For congenital forms there is currently no cure: management is based on information and guidance3. The optical aids studied so far do not restore normal colour vision3,9, while gene therapy, in the 2010 review, was a possibility studied in animals3.

Can women be colour-blind?

Yes, but much more rarely: about 0.4% of European women against 8% of men2. Many more are carriers, that is, have the alteration on one of the two X chromosomes without showing it: between 9 and 15% according to one estimate6.

Do colour-blind people see in black and white?

Almost never. In the most common forms some colours are confused, while complete loss of colour vision, achromatopsia, is rare1,4.

Can you become colour-blind as an adult?

Congenital colour blindness is present from birth, but an alteration of colours can appear during life because of diseases of the eye, the nervous system or general diseases7. A recent change should be assessed by the ophthalmologist.

Colour blindness is frequent and, in its most common forms, mild2,4. Knowing about it serves mainly two purposes: understanding why certain colours cause confusion, so as to organise oneself at school and at work, and recognising when an alteration in colours is not the usual one but a new change to have assessed3,7.

Sources

  1. Cvetković D, Cvetković D. [Inherited colour vision deficiencies–from Dalton to molecular genetics]. Srp Arh Celok Lek. 2005;133(11-12):521-7. doi:10.2298/sarh0512521c · PubMed 16758855
  2. Birch J. Worldwide prevalence of red-green color deficiency. J Opt Soc Am A Opt Image Sci Vis. 2012;29(3):313-20. doi:10.1364/JOSAA.29.000313 · PubMed 22472762
  3. Simunovic MP. Colour vision deficiency. Eye (Lond). 2010;24(5):747-55. doi:10.1038/eye.2009.251 · PubMed 19927164
  4. Swanson WH, Cohen JM. Color vision. Ophthalmol Clin North Am. 2003;16(2):179-203. doi:10.1016/s0896-1549(03)00004-x · PubMed 12809157
  5. Deeb SS, Kohl S. Genetics of color vision deficiencies. Dev Ophthalmol. 2003;37:170-87. doi:10.1159/000072046 · PubMed 12876837
  6. Oda S, Ueyama H, Tanabe S, Tanaka Y, Yamade S, Kani K. Detection of female carriers of congenital color-vision deficiencies by visual pigment gene analysis. Curr Eye Res. 2000;21(4):767-73. doi:10.1076/ceyr.21.4.767.5544 · PubMed 11120566
  7. Simunovic MP. Acquired color vision deficiency. Surv Ophthalmol. 2016;61(2):132-55. doi:10.1016/j.survophthal.2015.11.004 · PubMed 26656928
  8. Stoianov M, de Oliveira MS, Dos Santos Ribeiro Silva MCL, Ferreira MH, de Oliveira Marques I, Gualtieri M. The impacts of abnormal color vision on people’s life: an integrative review. Qual Life Res. 2019;28(4):855-862. doi:10.1007/s11136-018-2030-1 · PubMed 30443703
  9. Male SR, Shamanna BR, Bhardwaj R, Bhagvati C, Theagarayan B. Color vision devices for color vision deficiency patients: A systematic review and meta-analysis. Health Sci Rep. 2022;5(5):e842. doi:10.1002/hsr2.842 · PubMed 36189411 · PMC
  10. Hovis JK. Long wavelength pass filters designed for the management of color vision deficiencies. Optom Vis Sci. 1997;74(4):222-30. doi:10.1097/00006324-199704000-00024 · PubMed 9200166

Study titles are given in their original language of publication. The superscript numbers in the text refer to these sources; citation details come from PubMed (National Library of Medicine).

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