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Achromatopsia, also known as rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy.Historically, the name referred to monochromacy in general, but now typically refers only to an autosomal recessive congenital color vision condition.
Monochromacy (from Greek mono, meaning "one" and chromo, meaning "color") is the ability of organisms to perceive only light intensity without respect to spectral composition. Organisms with monochromacy lack color vision and can only see in shades of grey ranging from black to white. Organisms with monochromacy are called monochromats.
Color blindness is any deviation of color vision from normal trichromatic color vision (often as defined by the standard observer) that produces a reduced gamut. Mechanisms for color blindness are related to the functionality of cone cells , and often to the expression of photopsins , the photopigments that 'catch' photons and thereby convert ...
By comparison, every color in a trichromat's gamut can be evoked with a combination of monochromatic light and white light. Dichromacy in humans is a color vision deficiency in which one of the three cone cells is absent or not functioning and color is thereby reduced to two dimensions. [1]
This syndrome is not just a phenomenon, but a neurological disorder, where a person experiences constant visual disturbances, regardless of lighting conditions. Visual snow syndrome is often linked to heightened neural sensitivity in the visual system and may require diagnosis and treatment, as it could be associated with underlying eye ...
Color vision is categorized foremost according to the dimensionality of the color gamut, which is defined by the number of primaries required to represent the color vision. This is generally equal to the number of photopsins expressed: a correlation that holds for vertebrates but not invertebrates .
The main symptom is loss of vision, with colors appearing subtly washed out in the affected eye. A pale disc is characteristic of long-standing optic neuropathy. In many cases, only one eye is affected and a person may not be aware of the loss of color vision until the examiner asks them to cover the healthy eye.
Cerebral achromatopsia is a type of color blindness caused by damage to the cerebral cortex of the brain, rather than abnormalities in the cells of the eye's retina.It is often confused with congenital achromatopsia but the underlying physiological deficits of the disorders are completely distinct.