Improving Discrimination in Color Vision Deficiency by Image Re-Coloring [PDF]
Sensors, 2019 People with color vision deficiency (CVD) cannot observe the colorful world due to the damage of color reception nerves. In this work, we present an image enhancement approach to assist colorblind people to identify the colors they are not able to distinguish naturally.
Huei‐Yung Lin +2 more
europepmc +8 more sources
Potential value of color vision aids for varying degrees of color vision deficiency [PDF]
Optics Express, 2022 Red–green color vision deficiency (CVD) is the most common single locus genetic disorder in humans, affecting approximately 8% of males and 0.4% of females [G. H. M. Waaler, Acta Ophthalmol. 5, 309 (2009)10.1111/j.1755-3768.1927.tb01016.x]; however, only about 1/4 of CVD individuals are dichromats who rely on only two cone types for color vision.
Dragos Rezeanu +3 more
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Impact of color vision deficiency on the quality of life in a sample of Indian population: Application of the CVD-QoL tool [PDF]
Indian J Ophthalmol, 2023 Shiva Ram Male +5 more
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Wearable Improved Vision System for Color Vision Deficiency Correction [PDF]
IEEE Journal of Translational Engineering in Health and Medicine, 2017 Color vision deficiency (CVD) is an extremely frequent vision impairment that compromises the ability to recognize colors. In order to improve color vision in a subject with CVD, we designed and developed a wearable improved vision system based on an augmented reality device.
MELILLO, Paolo +8 more
openaire +8 more sources
Prevalence of color vision deficiency among Chinese college students and their quality of life [PDF]
Int J Ophthalmol, 2023 Jing-Ge Gao
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Genetic testing for color vision deficiency [PDF]
The EuroBiotech Journal, 2017 Abstract We studied the scientific literature and disease guidelines in order to summarize the clinical utility of genetic testing for color vision deficiency (CVD). Deuteranopia affects 1 in 12 males and is inherited in an X-linked recessive manner. It is associated with variations in the OPN1LW (OMIM gene: 300822; OMIM disease: 303900)
Andi Abeshi +5 more
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Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency [PDF]
Invest Ophthalmol Vis Sci, 2016 Purpose: Mutations in the coding sequence of the L and M opsin genes are often associated with X-linked cone dysfunction (such as Bornholm Eye Disease, BED), though the exact color vision phenotype associated with these disorders is variable. We examined
Ahmed, ZM +20 more
core +2 more sources
Implications of inherited color vision deficiency on occupations: A neglected entity! [PDF]
Indian J Ophthalmol, 2021 Amithavikram R. Hathibelagal
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Color vision devices for color vision deficiency patients: A systematic review and meta‐analysis [PDF]
Health Sci Rep, 2022 Shiva Ram Male +4 more
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Image-enhanced endoscopy improves visibility of endoscopic images in individuals with color vision deficiency [PDF]
Endosc Int OpenAkiko Ohno +12 more
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