Gene and genotype frequencies of color blindness in Basrah population

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Authors: Kawthar K. Hassan, Jaafar M. Owaid, Muntaha Y. Yousief
Cited by: 0

Abstract

This document presents a scientific study investigating the prevalence and genetic frequency of color blindness among 2,760 primary and secondary students across various regions of Basrah, Iraq. Utilizing Ishihara color charts, the researchers found that 6.40% of males and 0.91% of females were color blind, with deutan being the most common deficiency type identified. The findings highlight a significant lack of awareness regarding this condition in the population and establish a total colorblind allele frequency of 0.084

Fields of Study & Subjects

Ophthalmology and Visual Impairment Studies Retinal Development and Disorders Visual perception and processing mechanisms

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
16 February 2026
Language
EN
Document type
Dataset