Colour Vision Deficiencies

Molecular genetics of colour vision deficiencies.

Common variation in colour vision exists among both colour normal and colour deficient subjects. Differences at a few amino acid positions that influence the spectra of the L and M cone pigments account for most of this variation. The genes encoding the L and M photopigments are arranged in head-to-tail arrays on the X-chromosome, beginning with the L and followed by one or more M pigment genes...

Colour vision deficiencies in Alzheimer's disease.

OBJECTIVE visual disorders are among the earliest symptoms of Alzheimer's disease. It is, however, still controversial as to whether Alzheimer's disease impairs colour vision. In this study, colour vision of Alzheimer's disease patients was tested using the Ishihara test and the PV-16 choice test. The latter test, primarily designed for children, was chosen in order to avoid problems due to cog...

Colour-Vision and Colour-Blindness

Colour vision

The immense range of colours that we see belies the relative simplicity of the system underlying colour vision. We see colours because each of the three distinct types of cone photoreceptor in our retinae is sensitive to a different range of wavelengths of light. The L, M and S cones, colloquially called red (R), green (G), and blue (B), are selective for long, middle and short wavelengths, res...

Colour vision

Editorial Colour vision 2006 is an important bicentenary for the Ulster Medical Society. In 806, the Belfast Medical Society was founded and the later formation of the Belfast Clinical and Pathological Society in 853, allowed amalgamation of both societies to form the current Ulster Medical Society in 862. The vision of the early founders of the Belfast Medical Society, was far sighted, and som...