Inability to see specific colors The term color blind does not mean that objects are seen only in black and white Total color blindness is very rare There are many types and degrees of color blindness ID: 911284
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Slide1
VISUAL DEFECTS 3
Slide2COLOR BLINDNESS
Inability to see specific colors
The term ‘color blind’ does not mean that objects are seen only in black and white.
Total
color blindness is very rare.
There
are many types and degrees of color blindness.
The
most appropriate term for color blindness is
deficiency of color vision.
The
Trichromatic
theory explains this phenomenon very well
Color blindness or color vision deficiency is the inability to perceive differences between some of the colors that others can distinguish.
It is most often of genetic nature, but may also occur because of eye, nerve, or brain damage, or exposure to certain chemicals
.
Two types ; Acquired and Inherited
Congenital
/ inherited deficiencies
are due to the inborn abnormality of cone photoreceptor cells
Acquired
deficiencies results any time after birth___ occur due to the disorders that affect the eye or/ and the brain
In
both of these deficiencies, people experience colors differently from those with normal
trichromatic
color vision
Slide3CAUSES FOR ACQUIRED COLOR BLINDNESS
1. Trauma
Injury
to eye due to accidents or strokes results in
color blindness
.
2. Chronic Diseases
Color
blindness is caused by chronic diseases such as:
i
. Glaucoma
ii
. Degeneration of macula of eye iii. Retinitis
iv
. Sickle cell anemia
v
. Leukemia vi. Diabetes
vii
. Liver diseases
viii
. Parkinson disease ix. Alzheimer disease
x
. Multiple sclerosis.
3. Drugs
Frequent
use of some drugs leads to color blindness:
i
. Antibiotics
ii
. Antihypertensive drugs iii.
Anti-tuberculosis drugs
Barbiturates
v
. Drugs used to treat psychological
problems and
neural disorders.
4. Toxins
Industrial
toxins or strong chemicals cause color blindness. Common substances causing color blindness are:
i
. Fertilizers
ii
. Carbon monoxide
iii
. Carbon disulfide
iv
. Chemicals with high lead content.
5. Alcoholism
Chronic
alcoholism results in color blindness.
6. Aging
Color
blindness can occur after 60 years of age due
to various
changes in eye.
Slide4There
are three types of inherited or congenital color vision deficiencies:
monochromacy
,
dichromacy
,
anomalous
trichromacy
.
Monochromacy
,
It is also
known as "total color blindness," is the lack of ability to distinguish colors; caused by cone defect or absence.
Monochromacy
occurs when two or all three of the cone pigments are missing and color and lightness vision is reduced to one dimension.
Rod
monochromacy
(
achromatopsia
) is an exceedingly rare,
nonprogressive
inability to distinguish any colors as a result of absent or nonfunctioning retinal cones.
It is associated with light sensitivity (photophobia), involuntary eye oscillations (
nystagmus
), and poor vision.
Cone
monochromacy
is a rare total color blindness that is accompanied by relatively normal vision,
electoretinogram
, and
electrooculogram
.
Slide5Slide6Dichromacy
It is
a moderately severe color vision defect in which one of the three basic color mechanisms is absent or not functioning.
It is hereditary and, in the case of
Protanopia
or
Deuteranopia
, sex-linked, affecting predominantly males.
Dichromacy
occurs when one of the cone pigments is missing and color is reduced to two dimensions.
Protanopia
is a severe type of color vision deficiency caused by the complete absence of red retinal photoreceptors.
It is a form of
dichromatism
in which red appears dark. It is hereditary, sex-linked, and present in 1% of males.
Deuteranopia
is a color vision deficiency in which the green retinal photoreceptors are absent, moderately affecting red-green hue discrimination.
It is a form of
dichromatism
in which there are only two cone pigments present.
It is likewise hereditary and
sexlinked
.
Tritanopia
It is a very rare color vision disturbance in which there are only two cone pigments present and a total absence of blue retinal receptors.
Slide7Slide8Anomalous
trichromacy
is a common type of inherited color vision deficiency, occurring when one of the three cone pigments is altered in its spectral sensitivity. This results in an impairment, rather than loss, of
trichromacy
(normal three-dimensional color vision).
Protanomaly
is a mild color vision defect in which an altered spectral sensitivity of red retinal
receptors.
perception for red is weak. So to appreciate red color, the person requires more intensity of red than a normal person.
It
is hereditary, sex-linked, and present in 1% of males.
Deuteranomaly
, caused by a similar shift in the green retinal receptors, is by far the most common type of color vision deficiency, mildly affecting red-green hue discrimination in 5% of males. It is hereditary and sex-linked.
Tritanomaly
is a rare, hereditary color vision deficiency affecting blue-yellow hue discrimination. Unlike most other forms, it is not sex-linked.
Slide9Slide10Slide11TESTS FOR COLOR
BLINDNESS
Three
methods are available to determine the color blindness:
1. By using Ishihara color charts
2. By using Holmgren colored wool
3
. By using
Edridge
-Green lantern.