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Assessment of inherited colour vision defects in clinical practice
Abstract
Background Colour vision deficiency (CVD) has a high prevalence and is often a handicap in everyday life. Those who have CVD will be better able to adapt and make more informed career choices, if they know about their deficiency. The fact that from 20 to 30 per cent of adults with abnormal colour vision do not know they have CVD suggests that colour vision is not tested as often as it should be. This may be because of practitioner uncertainty about which tests to use, how to interpret them and the advice that should be given to patients on the basis of the results. The purpose of this paper is to recommend tests for primary care assessment of colour vision and provide guidance on the advice that can be given to patients with CVD. Methods The literature on colour vision tests and the relationship between the results of the tests and performance at practical colour tasks was reviewed. Results The colour vision tests that are most suitable for primary care clinical practice are the Ishihara test, the Richmond HRR 4th edition 2002 test, the Medmont C-100 test and the Farnsworth D15 test. These tests are quick to administer, give clear results and are easy to interpret. Tables are provided summarising how these tests should be interpreted, the advice that can be given to CVD patients on basis of the test results, and the occupations in which CVD is a handicap. Conclusion Optometrists should test the colour vision of all new patients with the Ishihara and Richmond HRR (2002) tests.…
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“Moreover, the deutan and protan individuals working with telecommunications and electric cables can recognize the blue and white wires but will be uncertain about the red, orange, brown and green.6”
From Prevalence and gene frequency of color vision impairments among children of six populations from North Indian region (2015) · cites this paper as [6]
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“In traffc signals, for deuteranope and protanope persons, the signals are less obvious, making handicap to perceive the signals.”
From Prevalence and gene frequency of color vision impairments among children of six populations from North Indian region (2015) · cites this paper as [6]
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Metadata
- Authors
- Cole, B. L.
- Affiliations
- Department of Optometry and Vision Sciences, The University of Melbourne
- Venue
- Clinical and Experimental Optometry
- Publisher
- Informa UK Limited
- Published
- 2007-05
- Volume
- 90
- Issue
- 3
- Pages
- 157-175
- ISSN
- 0816-4622
- 1444-0938
- Cited by
- 116
- References
- 0
- Language
- en
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