Color vision deficiency
Color vision deficiency (CVD) is a defect of vision with disability to distinguish colors. Color vision deficiency can be divided into the two categories, congenital and acquired. Congenital color vision deficiency divided into anomalous trichromacy, dichromacy and monochromacy. The most common cong...
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Format: | Article |
Language: | fas |
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Golestan University of Medical Sciences
2016-12-01
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Series: | مجله دانشگاه علوم پزشکی گرگان |
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Online Access: | http://goums.ac.ir/journal/browse.php?a_code=A-10-1-938&slc_lang=en&sid=1 |
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author | M Mahjoob M H Ostadimoghaddam H S Heydarian |
author_facet | M Mahjoob M H Ostadimoghaddam H S Heydarian |
author_sort | M Mahjoob M |
collection | DOAJ |
description | Color vision deficiency (CVD) is a defect of vision with disability to distinguish colors. Color vision deficiency can be divided into the two categories, congenital and acquired. Congenital color vision deficiency divided into anomalous trichromacy, dichromacy and monochromacy. The most common congenital CVD was deuteranomalous that mode of inheritance is X linked recessive occurring mostly in males. Acquired CVD can occur as a direct result of illness or any related medicine. Color perception changes in acquired CVD may be secondary to primary ocular disease, drug side effect, or serious systemic disease such as diabetes. Dystrophy of cone, types of maculopathy, crystalline lens changes associated with aging, diabetes, glaucoma, optic nerve diseases and traumatic brain injuries can cause CVD. For acquired CVD, type of defect may not be easy to classify; nevertheless, predominantly is tritanopia and type and severity of the defect fluctuates during of disease. It has been suggested that human evolution to industrialized civilization has led to an increased prevalence of CVD in most population. An acquired CVD can reflect a deficiency in color information processing at anywhere along the related visual pathway, from the photoreceptors to the cortex. Sometimes, assessment of color vision can be helpful to detect a visual impairment in early stages. |
first_indexed | 2024-12-12T04:41:26Z |
format | Article |
id | doaj.art-34e0b687567248eab66e750120d8d1b8 |
institution | Directory Open Access Journal |
issn | 1562-4765 2008-4080 |
language | fas |
last_indexed | 2024-12-12T04:41:26Z |
publishDate | 2016-12-01 |
publisher | Golestan University of Medical Sciences |
record_format | Article |
series | مجله دانشگاه علوم پزشکی گرگان |
spelling | doaj.art-34e0b687567248eab66e750120d8d1b82022-12-22T00:37:48ZfasGolestan University of Medical Sciencesمجله دانشگاه علوم پزشکی گرگان1562-47652008-40802016-12-0118418Color vision deficiencyM Mahjoob M0H Ostadimoghaddam H1S Heydarian2 Ph.D Candidate in Optometry, Refractive Errors Research Center, Department of Optometry, School of Paramedical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran Professor, Refractive Errors Research Center, Department of Optometry, School of Paramedical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran Ph.D Candidate in Optometry, Refractive Errors Research Center, Department of Optometry, School of Paramedical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran Color vision deficiency (CVD) is a defect of vision with disability to distinguish colors. Color vision deficiency can be divided into the two categories, congenital and acquired. Congenital color vision deficiency divided into anomalous trichromacy, dichromacy and monochromacy. The most common congenital CVD was deuteranomalous that mode of inheritance is X linked recessive occurring mostly in males. Acquired CVD can occur as a direct result of illness or any related medicine. Color perception changes in acquired CVD may be secondary to primary ocular disease, drug side effect, or serious systemic disease such as diabetes. Dystrophy of cone, types of maculopathy, crystalline lens changes associated with aging, diabetes, glaucoma, optic nerve diseases and traumatic brain injuries can cause CVD. For acquired CVD, type of defect may not be easy to classify; nevertheless, predominantly is tritanopia and type and severity of the defect fluctuates during of disease. It has been suggested that human evolution to industrialized civilization has led to an increased prevalence of CVD in most population. An acquired CVD can reflect a deficiency in color information processing at anywhere along the related visual pathway, from the photoreceptors to the cortex. Sometimes, assessment of color vision can be helpful to detect a visual impairment in early stages.http://goums.ac.ir/journal/browse.php?a_code=A-10-1-938&slc_lang=en&sid=1Color vision deficiencyAnomalous trichromacyDichromacyMonochromacy |
spellingShingle | M Mahjoob M H Ostadimoghaddam H S Heydarian Color vision deficiency مجله دانشگاه علوم پزشکی گرگان Color vision deficiency Anomalous trichromacy Dichromacy Monochromacy |
title | Color vision deficiency |
title_full | Color vision deficiency |
title_fullStr | Color vision deficiency |
title_full_unstemmed | Color vision deficiency |
title_short | Color vision deficiency |
title_sort | color vision deficiency |
topic | Color vision deficiency Anomalous trichromacy Dichromacy Monochromacy |
url | http://goums.ac.ir/journal/browse.php?a_code=A-10-1-938&slc_lang=en&sid=1 |
work_keys_str_mv | AT mmahjoobm colorvisiondeficiency AT hostadimoghaddamh colorvisiondeficiency AT sheydarian colorvisiondeficiency |