Abstract
Congenital red-green colour deficiency is an X-linked inherited disorder more frequently encountered in males compared to females. Screening of coour deficiency is crucial in various occupations, at times to safeguard colour deficient individual as well as vulnerable population. Acquired colour deficiency is seen in multiple inherited retinal photopigment disorders, vascular retonopathies and optic nerve disorders. Multiple tests have been devised to detect, classify and grade colour deficiency, each having a specific purpose. Tinted spectacles and contact lenses have been tried to rehabilitate colour deficient individuals with limited success.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
