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Prevalence of color vision deficiency in Qazvin
Zahedan Journal of Research in Medical Sciences. 2014; 16 (1): 91-93
en Inglés | IMEMR | ID: emr-169196
ABSTRACT
Color vision deficiency [CVD] is an X chromosome-linked recessive autosomal dominant. Determine the prevalence of color blindness in Qazvin population. In a cross sectional study color vision deficiency examined in 1853 individuals with age 10-25 years old who participated in private clinics and eye clinic of Bu-Ali hospital in Qazvin in 2010. The screening of color vision deficiency was performed using Ishihara test. Data were analyzed by SPSS-16 with chi[2] test with p<0.05. Mean age of participant was 17.86 +/- 4.48 years. 59.5% of them were female. 3.49% of the total population had color vision deficiency that 0.93% and 2.56% were female and male respectively. Color vision deficiency must be noticed by decision makers in health field for screen planning
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Índice: IMEMR (Mediterraneo Oriental) Tipo de estudio: Estudio de prevalencia Idioma: Inglés Revista: Zahedan J. Res. Med. Sci. Año: 2014

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Índice: IMEMR (Mediterraneo Oriental) Tipo de estudio: Estudio de prevalencia Idioma: Inglés Revista: Zahedan J. Res. Med. Sci. Año: 2014