What are the two main theories of colour vision?
Young–Helmholtz proposes three primary colours (red, green, blue) at the photoreceptor level, while Hering proposes opponent pairs and explains afterimages.
What are the key features of inherited colour vision defects?
These defects are typically genetic and stable over time.
What are confusion loci?
Lines plotted on a CIE diagram representing colours that appear identical
In anomalous trichromats, these lines are shorter and do not span the full colour range.
Differentiate protan, deutan, and tritan defects.
Each defect has specific confusion points on the CIE diagram.
What are monochromats?
They are rare and may experience reduced visual acuity, photophobia, and nystagmus.
What are dichromats?
They perceive a limited range of colours and exhibit confusion loci.
What are trichromats?
They can range from very mild to nearly as severe as a dichromat.
What are extreme anomalous trichromats?
Individuals with abnormal medium and long wavelength photopigments
Their matching range on an anomaloscope extends to both sides of the normal range.
What is the prevalence of colour vision defects?
The sex difference is due to X-linked inheritance of protan and deutan defects.
What are the key features of acquired colour vision defects?
These defects affect males and females equally.
Why is acquired colour vision deficiency difficult to classify?
Multiple classification systems exist
The defect can change as the underlying pathology progresses.
What is Verriest’s classification of acquired colour vision defects?
Each type has specific characteristics regarding visual acuity and colour loss.
What is Köllner’s rule?
Blue–yellow defects are associated with retinal disorders
Red–green defects are associated with optic nerve disease, with many exceptions.
Give examples of pathologies causing acquired colour vision defects.
Other conditions include retinal vascular disorders and glaucoma.
What is the key difference between inherited and acquired colour vision defects?
Inherited defects are stable, while acquired defects change over time.
What colour defect is most commonly seen in acquired conditions?
Blue–yellow defects
These defects often indicate retinal pathology.
How does visual acuity differ between inherited and acquired colour vision defects?
This reflects the underlying pathology of acquired defects.
How does symmetry differ between inherited and acquired colour vision defects?
This can lead to monocular differences.
How does progression differ between inherited and acquired colour vision defects?
This is due to the underlying pathology.
What are acquired colour abnormalities due to brain injury?
These conditions are associated with damage to specific brain areas.
What is chromatopsia?
A condition where vision appears tinted with a colour
Colour discrimination remains normal.
What is cyanopsia and when does it occur?
Blue-tinted vision, commonly occurring after cataract removal
It can also occur as a side effect of Viagra.
What are the different types of chromatopsia and their causes?
Each type has specific causes, often related to medications or conditions.
What illumination is recommended for colour vision testing?
Illuminant C is recommended
MacBeth lamp is commonly used for tests with pigment colours.