colour blindness drka

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    COLOUR BLINDNESS

    Skill labFakultas Kedokteran

    Universitas Muhammadiyah Yogyakarta

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    Color blindness or color visiondeficiency is the inability toperceive differences between some

    of the colors that others can

    http://en.wikipedia.org/wiki/Color_visionhttp://en.wikipedia.org/wiki/Color_vision
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    normal

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    protanope

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    deuteranope

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    tritanope

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    Total colour-blindness

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    retina

    Normally, there are three kinds

    ofcones (each one sensitive to aspecific range of wavelengths):

    "red" cones (64%)

    "green" cones (32%)"blue" cones (2%)

    The normal human retina contains two kinds of light sensitivecells: the rod cel ls (active only in low l ight) and the conecel ls (active in normal dayl ight and responsible forcolor perception).

    The different kinds of inherited color blindness result frompartial or complete loss of function of one or more of thedifferent cone systems.

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    Blue conesabsent incentralfovea

    Red, greenand blue conesensitivity vs.wavelength

    curves

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    CAUSES

    GENETIC : sex-linked recessive / X-Linked

    mutations from at least 19different chromosomes and 56different genes

    Inherited color blindness congenital, non congenital (conedystrophy)

    Others : trauma, radiation, maculardegeneration

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    Females

    X

    N

    X

    N

    =

    Normal

    XN

    Xn

    =

    Carrier

    Xn

    Xn

    =

    affected

    Males

    XN

    Y =

    Normal

    Xn

    Y =

    affected

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    BUTA WARNA

    BUTA WARNATOTAL

    BUTA WARNAPARSIAL

    Monochromacy

    Rod monochromacy,

    Cone monochromacy

    Achromatopsia

    Rod monochromacy,

    Color Agnosia

    cerebral Achromatopsi

    Dichromacy

    Protanopia

    Deuteranopia

    Tritanopia

    Anomalous trichromacy

    Protanomaly

    Deuteranomaly

    Tritanomaly

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    EPIDEMIOLOGIColor Deficiency Males Females

    Protanopia 1% 0.01%Deuteranopia 1% 0.01%

    Protanomaly 1% 0.01%

    Deuteranomaly 5% 0.4%Overall (red-

    green)8% 0.5%

    Tritanopia 0.008% 0.008%

    Tritanomaly Rare Rare

    Rod

    monochromatism

    Rare Rare

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    Monochromacy

    is the condition of possessing only a single channel forconveying information about color. Monochromatspossess a complete inability to distinguish any colorsand perceive only variations in brightness.

    Rod monochromacy, frequently called achromatopsia,where the retina contains no cone cells, so that in additionto the absence of color discrimination, vision in lights ofnormal intensity is difficult.

    Cone monochromacy is the condition ofhaving bothrods and cones, but only a single kind of cone. A conemonochromat can have good pattern vision at normaldaylight levels, but will not be able to distinguish

    hues.

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    protanopia, deuteranopia,protanomaly, and deuteranomaly

    SEX-LINKED

    have difficulty with discriminatingred and green hues.

    Red-green colorblindness

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    PROTANOPIA (dichromacy)

    1% of males

    (no red cones; only green andblue)

    unable to distinguish between colorsin the green-yellow-red section of thespectrum

    the brightness of red, orange, andyellow is much reduced compared tonormal.

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    17

    B RG

    437 nm

    533 nm

    Protan Dichromat(no red cones; only green and blue)

    1% ofMales

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    18

    B G

    437 nm

    533 nm

    Protan Dichromat(no red cones; only green and blue)

    1% of Males (there is no redcurve)

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    Protanomaly

    Protanomaly (1% of males, 0.01% offemales)

    Having a mutated form of the long-wavelength (red) pigment

    whose peak sensitivity is at a shorterwavelength than in the normal retina,

    less sensitive to red light than normal.

    reds to reduce in intensity to the pointwhere they can be mistaken for black. Both protanomaly and deuteranomaly

    are carried on the X chromosome.

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    20

    B RG

    437 nm

    533 nm

    Protanomalous(red shifted toward green)

    1% ofMales

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    Deuteranopia(dichromacy)

    1% of males

    no green cones; only red andblue

    unable to distinguish between colorsin the green-yellow-red section of thespectrum.

    The deuteranope suffers the samehue discrimination problems as theprotanope

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    24

    B RG

    437 nm 564 nm

    Deutan Dichromat(no green cones; only red and blue)

    1% ofMales

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    25

    B R

    437 nm 564 nm

    Deutan Dichromat(no green cones; only red and blue)

    1% of Males (there is nogreen curve)

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    Deuteranomaly

    most common - 6% of males, 0.4% of females Having a mutated form of the medium-wavelength

    (green) pigment. The medium-wavelength pigment is shifted towards the red

    end of the spectrum resulting in a reduction in sensitivity tothe green area of the spectrum.

    Unlike protanomaly the intensity of colors is unchanged The deuteranomalous person is considered "green weak".

    For example, in the evening, dark green cars appear to beblack to Deuteranomalous people.

    Similar to the protanomates, deuteranomates are poor at

    discriminating small differences in hues in the red,orange, yellow, green region of the spectrum. One very important difference between deuteranomalous

    individuals and protanomalous individuals isdeuteranomalous individuals do nothave the loss of"brightness" problem.

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    27

    B RG

    437 nm 564 nm

    Deuteranomaly(green shifted toward red)

    5% ofMales

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    Blue-yellow colorblindness

    Those with tritanopia and tritanomaly have difficultywith discriminating blue and yellow hues.

    Color blindness involving the inactivation of the short-wavelength sensitive cone system (whose absorptionspectrum peaks in the bluish-violet) is called tritanopiaor, loosely, blue-yellow color blindness. The tritanopes

    neutral point occurs near a yellowish 570 nm; green isperceived at shorter wavelengths and red at longerwavelengths.

    Mutation of the short-wavelength sensitive cones is calledtritanomaly.

    Tritanopia is equally distributed among males and females. Jeremy H. Nathans (with the

    Howard Hughes Medical Institute) proved that the genecoding for the blue receptor lies on chromosome 7, which isshared equally by males and females.

    Therefore it is not sex-linked. Blue color blindness is caused by a simple mutation in this

    gene.[21]

    http://en.wikipedia.org/wiki/Howard_Hughes_Medical_Institutehttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Howard_Hughes_Medical_Institute
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    The Series of PlatesDesign as aTest for Colour-Blindness

    By

    SHINOBU ISHIHARA M.D., Dr. Med. Sc.

    Emeritus Professor of Ophtalmology, Tokyo University,

    Member of the Japan Academy

    http://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindnesshttp://en.wikipedia.org/wiki/Color_blindness