Colour blindness ppt by meera qaiser

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COLOUR BLINDNES S Presented by: Meera Qaiser Presented to: Miss Irum Anjum Subject: Essentials of genetics Major: Biotechnology Semester: 4 th

description

presentation on color blindness

Transcript of Colour blindness ppt by meera qaiser

Page 1: Colour blindness ppt by meera qaiser

COLOUR BLINDNE

SSPresented by: Meera Qaiser

Presented to: Miss Irum Anjum

Subject: Essentials of genetics

Major: Biotechnology

Semester: 4th

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WHAT IS COLOUR BLINDNESS?

Color blindness means that you have trouble

seeing red, green, or blue or a mix of these

colors. It’s rare that a person sees no color at

all.

Color blindness is also called a color vision

problem.

A color vision problem can change your life.

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CAUSES OF COLOUR BLINDNESS:1. Usually genetic condition. Red/Green or Blue colour blindness is passed

down from parents. The gene responsible is on X chromosome. mutations capable of causing color blindness

originate from at least 19 different chromosomes and many different genes

More males are affected the females are basically carrier

There is 50% chance of mother passing this condition to her son

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o Inherited condition maybe due to following…..

o In our eye there are two types of light sensitive

cell

1. Rods

2. cones

o Both found in retina which is a layer at the back

of eye it processes images.

o The rods are responsible for vision in night as

work in low light condition ( cannot distinguish

different wavelength of light)

o The cones are responsible for color discrimination

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CONTINUEDo there are three types of cones

o ( differ on the basis of photoreceptor protein

they make)

1. L-cones sense long wavelenght ( red light)

2. M-cones sense medium wavelength ( green

light)

3. S-cones sense shorter wavelenght ( blue

light )

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When you see an object light enters your eye and stimulates the cone cells

Your brain interpret the

signals from the cone cell

and enable you to see the

colour of object They work together

enabling us to see whole spectrum of colours.

Faulty cones thus are responsible for color blindness

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2. Acquired color blindness:

Aging.

Eye problems, such as glaucoma, macular

degeneration, cataracts, or diabetic

retinopathy

Injury to the eye.

Side effects of some medicines.

If you have inherited colour blindness your

condition will stay the same throughout your

life – it won’t get any better or worse.

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TYPES OF COLOUR BLINDNESS

1. Trichromacy ( three colour vision )

- Normal colour vision

2. Anomalous trichomacy ( unusuall three colour

vision )

- See all three primary colour

- One colour is seen weakly

- Protanomaly ( l-cone defect ) red weak

- Deuteranamoly ( M-cone defect ) green weak

- Tritanomaly ( S-cone defect ) Blue weak

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3. Dichromacy ( two colour vision)

- See only two of three primary colours

- One cone is totally disfunctional or absent- Protanopia ( l-cone absent )- Detutranopia ( M-cone absent )- Tritanopia ( S-cone absent )

4. Rod monochromacy (no cones at all )- Sees no colour only shades of grey

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INHERITENCE PATTERN Red-green colour blindness is usually

inherited from parents It is passed from mother to son on 23rd

chromosome which is sex chromosome Chromosomes are the structure which

contains genes, they contain instructions for the development of cell tissues organ and if you are colour blind it means instructions for cone development are wrong

It may be missing or less sensitive Or pathway from cone to brain is not

developed properly

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For male to be color blind his X chromosome

should have the faulty gene

The female might have both X chromosomes

normal or one X chromosome might have faulty

gene but gene on other chromosome

compensates it so the female is carrier and

passes on faulty gene to her son so he is

colorblind

The daughter might be carrier or color blind if

her father is colorblind and mother is the carrier

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COLOR BLIND MAN NON COLOR BLIND WOMEN

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NON COLOR BLIND MAN COLOR BLIND CARRIER MOTHER

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COLOR BLIND MAN COLOR BLIND CARRIER WOMEN

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NON COLOUR BLIND MAN COLOUR BLIND WOMEN

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DIAGNOSIS It maybe difficult to detect in children with

inherited colour vsion deficiency as they don’t know whats wrong with them

If you have eye test with optometrist he should check your colour vision as a matter of routine

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ISHIARAS TEST

There are many tests available to measure colour vision defects but the most common is the Ishihara Plate test.

can test for red/green colour blindness but not blue colour blindness.

This is the test most likely to be used for routine colour vision screening in schools or medicals.

This test contains 38 plates of circles created by irregular coloured dots in two or more colours.

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PLATES FOR ISHIARAS TEST

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TREATMENT There is currently no treatment Colour filters or contact lenses can be used in

some situations to enhance the brightness between some colours

For acquired colour vision deficiency, once the cause has been established and treated, your vision may return to normal.

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PEOPLE LIVING WITH COLOUR BLINDNESS:

Colour blind people face many difficulties in everyday life

Problems can arise in even the most simple of activities including choosing and preparing food, gardening, sport, driving a car and selecting clothing.

Colour blind people can also find themselves in trouble because they haven’t been able to pick up a change in someone’s mood by a change in colour of their face

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REFERENCES http://www.webmd.com/eye-health/tc/color-

blindness-topic-overview

http://www.colourblindawareness.org/colour-blindness/colour-blindness-experience-it/

http://www.geteyesmart.org/eyesmart/diseases/color-blindness.cfm

http://www.colblindor.com/2010/03/02/what-is-color-blindness/

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Thankyou