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About ColorBlindness

 

 

 

Colorblindness

Colorblindness is a visual insufficiency that disables the capacity of distinguishing several colors. As a result of hereditary transmission, colorblindness drifts from a genetic deficiency associated with the X chromosome.

The condition is often called daltonism, named after John Dalton, the scientist who, in the XVIII century, first described the pathology and who was himself colorblind.

 

 

 

The first symptoms are detected at school age

The condition of colorblindness has a genetic origin related with X chromosome

 

Normal Vision

Colorblind Vision

 

Colorblindness affects approximately every 1 in 12 men and 1 in 200 women.

 

The first symptoms are detected early at school age normally related with difficulties or confusion acknowledging the different colors and already at this time the feel of social inadequacy is initiated, enhanced by the tease of the colleagues.

In time constraints are enhanced: the scope of professional possibilities decreases which may affect the personal fulfillment, while the feeling of non-integration increases.

 

 


Color Identification Mechanism and Colorblindness

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Hermann Von Helmholtz proposes a theory describing the organic mechanism responsible for the colorblind state in line with the studies of Thomas Young. The Young-Helmholtz theory, argue that the retina had specialized cells, named Cones, that were responsible for the color perception and the malfunction of these cells would cause colorblindness.

Cones are less sensitive to light than the other cells in the retina but allow the perception of color. They are also able to perceive finer detail and more rapid changes in images because their response times to stimuli is faster than those of rods.

Humans usually have three kinds of cones with different photoreceptive proteins, which have different response curves and thus respond to variation in color in different ways. Changes in the protein composition of Cones, implies different colorblind states.

 

Websites with useful information about colorblindness.

HTTPS://WWW.NHS.UK/CONDITIONS/COLOUR-VISION-DEFICIENCY/

HTTPS://WWW.COLOURBLINDAWARENESS.ORG/

HTTPS://WWW.COLOR-BLINDNESS.COM/

HTTPS://EN.WIKIPEDIA.ORG/WIKI/COLOR_BLINDNESS

HTTPS://ACROMATES.ORG/



Affects approximately every 1 in 12 men and 1 in 200 women.



Tests for color vision deficiency.

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There are several types of tests used to diagnose color blindness, the most used being:

  • The Ishihara test, where you're asked to identify numbers contained within images made up of different colored dots
  • Color arrangement, where you're asked to arrange colored objects in order of their different shades

There are online tests using similar techniques that may help detect a possible problem, but it's best to have a proper test at an optician if you have any concerns about your color vision.


 

 

THERE ARE DIFFERENT CONDITIONS

 

 

Deuteranopia


Affects hue discrimination in a similar way to protanopia, but without the dimming effect. Again, it is found in about 1% of the male population.

 

 

ProtanopiA


Is caused by the absence of red retinal photoreceptors and it results on difficulties distinguishing between blue and green and between red and green. It is present in 1% of males.

 

Tritanopia


A very rare color vision disturbance in which only the red and the green cone pigments are present, with a total absence of blue retinal receptors. Blues appear greenish, yellows and oranges appear pinkish, and purple colors appear deep red.

 

Monochromacy


Also known as "total color blindness", is the lack of ability to distinguish colors (and thus the person views everything as if it were on a black and white television); caused by cone defect or absence.

 

 

 

 

 

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