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Review
. 2019 Feb;42(2):177-188.
doi: 10.1016/j.jfo.2018.05.018. Epub 2019 Jan 29.

[Hereditary color vision deficiency: Physiology, classification, diagnosis and application to aeronautics]

[Article in French]
Affiliations
Review

[Hereditary color vision deficiency: Physiology, classification, diagnosis and application to aeronautics]

[Article in French]
M Marechal et al. J Fr Ophtalmol. 2019 Feb.

Abstract

Hereditary color vision deficiency affects 9% of men and 0.5% of women. It is often unrecognized and diagnosed late, which can interfere with the professional careers of these patients. Most color vision deficiencies are related to X chromosome involvement and concern the red-green chromatic axis. They are secondary to dysfunction of an L or M cone (protanomaly or deuteranomaly) or to the absence of an L or M cone (protanopia or deuteranopia). Color vision deficiency screening and assessment can be done by confusion tests or equalization tests, but also by ergonomic tests, professional tests that assess the aptitude for a given profession.

Keywords: Color vision tests; Deutan; Dyschromatopsia; Dyschromatopsie ;Tests de la vision des couleurs ;Physiologie ;Protan; Physiology; Protan.

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