Dyschromatopsy, Achromatopsia and Blue Cone Monochromatism; Pathophysiology, Clinical Findings, Diagnosis, and Treatment
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Abstract
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Abstract
Color vision is a complex perception caused by the stimulation of cone photoreceptors in the retina and the perception of this stimulation in the brain. Hereditary color vision deficiencies are caused by a defect in the functions of cone cells. Color vision deficiencies are named according to three different types of pigments contained in cones. These disorders, which are seen in high prevalence worldwide, are found more frequently in males. Contrary to thought, colored vision defects often affect daily life. Although it can be easily diagnosed with color vision tests and electrophysiological tests, current treatment options are limited and its success rate is low.
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Color vision is a complex perception caused by the stimulation of cone photoreceptors in the retina and the perception of this stimulation in the brain. Hereditary color vision deficiencies are caused by a defect in the functions of cone cells. Color vision deficiencies are named according to three different types of pigments contained in cones. These disorders, which are seen in high prevalence worldwide, are found more frequently in males. Contrary to thought, colored vision defects often affect daily life. Although it can be easily diagnosed with color vision tests and electrophysiological tests, current treatment options are limited and its success rate is low.
Key concepts: Achromatopsia, Color vision, Color Vision Defects, Perception, Neuroscience, Color perception test, Medicine, Retina