Color vision deficiency among biomedical students: a cross-sectional study
- PMID: 29950807
- PMCID: PMC6016265
- DOI: 10.2147/OPTH.S160110
Color vision deficiency among biomedical students: a cross-sectional study
Abstract
Purpose: To determine the prevalence of color vision deficiency (CVD) among first-cycle students of the Faculty of Medicine and Biomedical Sciences of the University of Yaoundé I.
Patients and methods: A cross-sectional descriptive study was carried out between October 1, 2015 and May 31, 2016. Distant visual acuity was measured and color vision test done for all consenting students. Ishihara's plates were used to test all the participants. Those who failed the test were tested with the Roth's 28 Hue test for confirmation of CVD and classification.
Results: A total of 303 students were included, among whom 155 were males (50.8%) and 148 were females (49.2%). The mean age was 20.2±2 years. Five students (1.6%) failed the Ishihara's plate testing. Roth's 28 Hue test confirmed CVD in 4 of those cases, giving a prevalence of 1.3%. There were equal numbers of protan and deutan CVD.
Conclusion: Despite its low prevalence among first-cycle students of the Faculty of Medicine and Biomedical Sciences, CVD screening should be performed in order to raise awareness, which will go a long way to help orientate the choice of future specialty.
Keywords: biomedical students; color vision deficiency; deutan; protan.
Conflict of interest statement
Disclosure The authors report no conflicts of interest in this work.
Figures
Comment in
-
Blind spots in medical students with color vision deficiency.Clin Ophthalmol. 2018 Sep 25;12:1875-1876. doi: 10.2147/OPTH.S178769. eCollection 2018. Clin Ophthalmol. 2018. PMID: 30310266 Free PMC article. No abstract available.
References
-
- Deeb SS. Molecular genetics of color-vision deficiencies. Vis Neurosci. 2004;21(3):191–196. - PubMed
-
- Henry GH, Cole BL, Nathan J. The inheritance of congenital tritanopia with the report of an extensive pedigree. Ann Hum Genet. 1963;27(3):219–231. - PubMed
-
- Krill AE, Smith VC, Pokorny J. Further studies supporting the identity of congenital tritanopia and hereditary dominant optic atrophy. Invest Ophthalmol. 1971;10(6):457–465. - PubMed
-
- Birch J. Worldwide prevalence of red-green color deficiency. J Opt Soc Am A Opt Image Sci Vis. 2012;29(3):313–320. - PubMed
-
- Ezangono Ndo MM. MD [Thesis] Yaounde: University of Yaounde I; 2010. Profil épidémiologique des dyschromatopsies héréditaires chez les enfants des trois écoles primaires de la ville de Douala [Epidemiological profile of congenital color vision deficiencies in children attending three primary schools in the city of Douala]
LinkOut - more resources
Full Text Sources
Other Literature Sources
