Biology IA
Biology IA
Biology IA
Topic question
How is color vision deficiency diagnosed and what are the background statistics of it?
Introduction
It's interesting to think how color vision really affects people and how they see things. Color vision really
affects people's lives and how they do things that are different from others. With all the research that I’ve
done for color deficiency, it amazes me that there are different ways that it’s caused, how it could be
treated and tested. This inability is really rare to some people and most don’t even know that they do have
it depending on if you ever got tested. Color blindness is a genetic condition, which means you are born
with it. Color blindness can also happen because of damage to your eye or your brain. And color vision
may get worse as you get older often because of cataracts. The background statistics of color deficiency
rely on what different things cause it, risk and how people live with it. A color vision problem can change
your life. It makes it harder to learn and read, and you may not be able to have certain careers. Many
young children get teased because of their condition, and few will believe what they are told. But people
with color blindness can and have learned to make up for their problems seeing color.
Exploration
Color vision deficiency is the inability to distinguish certain shades of color. The term "color blindness" is
also used to describe this visual condition, but very few people are completely color blind. The eye is a
difficult and complex piece of anatomy capable of determining everything from shapes, colors and to
details. There are many tasks the eye is able to perform, but one of the eye’s key tasks is to aid in the
determination of the many variations of color.[4] The brain is able to differentiate color based on the
different wavelengths that hit and are transmitted by the retina. This is because the cones that, in part,
make up the retina contain photopigments sensitive to short, medium and long wavelengths of light often
associated with the three primary colors red, blue and green. [5] Absorption of combinations of
Analysis
Color blindness affects approximately 1 in 12 men (8%) and 1 in 200 women in the world. In Britain this
means that there are approximately 3 million colour blind people who are mostly male. Researchers
studying red and green color blindness in the United Kingdom reported an average prevalence of only 4.7
percent in one group. Only 1 percent of Eskimo males are color blind. Approximately 2.9 percent of boys
from Saudi Arabia and 3.7 percent from India were found to have deficient color vision. Red/green color
blindness may slightly increase an affected person's chances of contracting leprosy. Preterm infants
exhibit an increased prevalence of blue color blindness. Achromatopsia has a prevalence of about one in
33,000 in the United States and affects males and females equally.
Types of color vision deficiency
The most common type of color blindness makes it hard to tell the difference between red and green.
Another type makes it hard to tell the difference between blue and yellow. Blue/yellow color blindness
can be observed only very rarely. Different studies diverge a lot in the numbers but as a rule of thumb you
could say one out of 10’000 persons is affected at most. In contrast to red/green color blindness tritan
defects are autosomal and encoded on chromosome 7. This means tritanopia and tritanomaly are not sex-
linked traits and therefore women and men are equally affected. People who are completely color blind
don’t see color at all in some cases but its pretty rare. Color blindness that is inherited is present in both
eyes and remains constant over an individual's entire life. Some cases of acquired color vision loss are not
severe, may appear in only one eye, and last for only a short time. Other cases tend to become worse with
time.
Data collected from ‘’The genetics of normal and defective color vision’’ article.[6]
This data that was collected was based on the percentages of different color vision defects from men and
women. This data proves how vision defects from the cones are based on the type of person who is being
diagnosed with this. The different types go for anyone from any gender or any type of person and what
they have. It goes more into the statistics and what exactly happens when someone is diagnosed with this
deficiency so you could understand how it works and possibly how to work with it.
These conditions occur in fewer than 1 in 10,000 people worldwide. Blue cone monochromacy is rarer
than the other forms of color vision deficiency, affecting about 1 in 100,000 people worldwide. Like red
or green color vision defects, blue cone monochromacy affects males much more often than females. The
Red/green and blue color blindness appear to be located on at least two different gene locations. The
majority of affected individuals are males. Females are carriers but are not normally affected. [2] This
indicates that the X chromosome is one of the locations for color blindness. Male offspring of females
who carry the altered gene have a 50 percent chance of being color-blind. [2] The rare female that has red
and green color blindness, or rarer still, blue color blindness, indicates there is an involvement of another
gene. As of 2004, the location of this gene was not yet identified.
mostly packed into the fovea centralis. By population, about 64% of the cones are red-sensitive, about
32% green sensitive, and about 2% are blue sensitive.[7] The "blue" cones have the highest sensitivity
and are mostly found outside the fovea. The shapes of the curves are obtained by measurement of the
absorption by the cones, but the relative heights for the three types are set equal for lack of detailed data.
[7] the different sensitivity levels indicate how the colors work through the eye and how it is being seen
from a person. There are fewer blue cones, but the blue sensitivity is comparable to the others, so there
must be some boosting mechanism. In the final visual perception, the three types seem to be comparable,
Color deficiency is an inherited condition caused by a common X-linked recessive gene, which is passed
from a mother to her son. Disease or injury that damages the optic nerve or retina can also cause loss of
color recognition. [1] Some diseases that can cause color deficits are:
● Diabetes
● Glaucoma
● Macular degeneration
● Alzheimer's disease.
● Parkinson's disease.
● Multiple Sclerosis.
● Chronic alcoholism.
● Leukemia.
To get tested or diagnosed for CVD is being tested through a doctor. During the test, your eye doctor will
show you a circle made of many different colored dots. The circle has a shape inside it that’s made out of
dots like a number, a letter, or a squiggly line. This shape is easy to see if you don’t have color blindness,
but people who are color blind have a hard time seeing it. There are different types of tests to take: color
plate test, anomaloscope test, & hue test which all indicate ways to check for CVD.
Charts of
Treatment and prevention
As of 2004 there is no treatment or cure for color blindness. Most color vision deficient persons
compensate well for their abnormality and usually rely on color cues and details that are not consciously
evident to persons with typical color vision. Inherited color blindness cannot be prevented. In the case of
some types of acquired color deficiency, if the cause of the problem is removed, the condition may
improve with time. But for most people with acquired color blindness, the damage is usually
permanent.There is no way to prevent genetic color blindness. There is no way to prevent acquired color
blindness that is associated with Alzheimer's disease, diabetes mellitus, leukemia, liver disease, macular
degeneration, multiple sclerosis, Parkinson's disease, sickle cell anemia, and retinitis pigmentosa.
Conclusion
Color deficiency is so important because people often overlook how much the inability to see certain
colors can change a person’s life. It affects everything from what jobs a color deficient person can do to
small choices like what that person would want to eat. Since color deficiency does not physically hurt a
human, those without color deficiency do not realize the person is being forced to adapt to a world in
which he or she cannot properly perceive a significant portion. Educating people both with and without
color deficiency of the effects of the problems, the gap between both perceptions can be significantly
lessened well towards others. Today, many changes and efforts are still being made to improve the
knowledge of color deficiency. In recent years, efforts have been made to make color deficiency tests
more accessible to the public. [4] One of the best methods of encouraging the public is through the use of
online tests such as the Color Vision Plate Test found on EnChroma (Schmeder, McPherson, and
Sheldon, n.d.). There are many online tests like this one are important because it encourages people of
this condition to seek help by allowing them to understand the problem as well as provide assistance
using the websites provided. Research is the best way to help anyone affected with color deficiency
regardless of severity because it widens the general public’s comprehension on the struggles a color
deficient person faces and encourages new solutions to avert everyday troubles.
sso=y#:~:text=People%20who%20are%20totally%20color,caused%20by%20injury%20or%20illness.
Source 2: https://www.nei.nih.gov/learn-about-eye-health/eye-conditions-and-diseases/color-
blindness/causes-color-blindness
Source 3: https://www.colourblindawareness.org/colour-blindness/inherited-colour-vision-deficiency/
Source 4:
https://www.2020mag.com/article/the-importance-of-understanding-color-vision-deficiency
Source 6: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3075382/
Source 7: http://hyperphysics.phy-astr.gsu.edu/hbase/vision/colcon.html