Congenital color vision deficiency has a higher prevalence among boys younger than 19 years of age and individuals of European ancestry.

Aims: To determine if asymptomatic carriers from a previously identified large pedigree of the Leber’s hereditary optic neuropathy (LHON) 11778 mtDNA mutation have colour vision deficits. Methods: As ...

This python package is a companion to the desktop application DaltonLens. Its main goal is to help the research and development of better color filters for people with color vision deficiencies. It ...

El daltonismo es una condición ocular que se caracteriza por la dificultad de percibir las longitudes de onda del color. La mayoría de los casos se desarrollan por causas genéticas, aunque también es ...

Accessibility: --no-colour flag for the colour blind and terminal purists (Don't hate I'm Deutan so trying to save people from my sh***y colour matching too) Clean Output: No more scrolling through 50 ...