Colour Vision defects Flashcards

1
Q

What is anomalous trichromacy?

A

Impairment of normal colour vision where one of the cones is altered (defected) in its spectral sensitivity

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2
Q

In the deficiency protanomaly what mechanism and characteristics do they inherit?
which cones are affected?
what is the inheritance pattern?
and what is the prevalence?

A
  1. Reduced sensitivity to red light due to defective L (red) cone pigment May confuse white with green and confuse reds, yellows and greens but loss of colour discrimination varies greatly between individuals. Reduced sensitivity to red light.
  2. RED
  3. X linked recessive
  4. 1.08% of the population, 1% in Men and 0.03% in Women
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3
Q

In the deficiency Deuteranomaly what mechanism and characteristics do they inherit?
which cones are affected?
what is the inheritance pattern?
and what is the prevalence?

A
  1. Reduced sensitivity to green light due to defective M (green) cone pigment May confuse white with green and confuse reds, yellows and greens but loss of colour discrimination varies greatly between individuals.
  2. Green
  3. X linked recessive
  4. 4.63% in the population 5% in Men 0.03% in Women
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4
Q

In the deficiency Tritanomaly what mechanism and characteristics do they inherit?
which cones are affected?
what is the inheritance pattern?
and what is the prevalence?

A
  1. Reduced sensitivity to blue light due to defective S (blue) cone pigment Loss of colour discrimination for blues, blue – greens and greens.
  2. Blue
  3. autosomal dominant
  4. 1 in 500 very rare
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5
Q

What is the prevalence of protanopia?

A

1.01% in the population, 1% in men, 0.01% in Women

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6
Q

what is the prevalence of deutanopia?

A

1.27% in the population, 1% in men, 0.01% in Women

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7
Q

What is Kollner’s rule? what conditions do not follow this rule?

A

This rule states that outer retinal diseases and media changes result in blue-yellow color defects, while diseases of the inner retina, optic nerve, visual pathway, and visual cortex will result in red-green defects.

There are exceptions to Köllner’s rule, notably glaucoma, which is an optic nerve disorder, and is usually associated with blue-yellow defects in the initial phase, following which red-green defects later develop.

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8
Q

What does a Nagle Anomaloscope differentiate between?

Explain the test and findings

A

Differentiates between

  • Dichromats and anomalous trichromats
  • Dichromats; all yellow intensities are matched
  • Anomalous trichromats; range of matches reflects severity
  • Protanopes have more red
  • Deutanopes have more green
  • Normal finds only one match
  • Tritanopia not tested
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9
Q

What is a Ishihara test?
Explain the test ad findings?
what type of plates are there?

A

Colour Discrimination

  • Standard illuminant C
  • 38 plate test (or 24)
  • 1plateperpage
  • 2demonstration/malingerer plates
  • Positive plates, ie sees alternative number
  • False negative plates, ie sees nothing
  • 4 false positive plates, ie sees #
  • 4 plates, differentiate Protan/Deutan
  • 12 plates with lines
  • To pass 24 plate ishihara, you can misread only 2 or less
  • To pass 38 plate ishihara, you can misread only 3 or less

For occupational testing, if a patient fails the Ishihara, review the city university test or the D15

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10
Q

What does the D15 saturated and desaturated test for?

what would a protan, deutan and tritan result look like?

A

D15 (Saturated and Desaturated)

Colour Matching

  • Selection from Farnsworth
  • Desaturated = increased sensitivity
  • Discs are numbered on reverse
  • The 15 Caps are orientated on the CIE Chromaticity diagram to emphasise the colour confusion for the three deficiencies (Protan, Deutan and Tritan)
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11
Q

What is possible management/ counselling for a colour deficient patient?

A

• Chromagen lenses (although limitations)

o Enhances colour perception rather than treating CVD

§ Shifts the wavelength of light that the individual can now see

o Cannot be used during CV testing for occupational purposes

• Genetic Counselling

o Although there is no cure for this condition, genetic counselling can indicate the chances for a CVD being passed on to the patient’s children

· Can prepare for such outcome

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