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Color blindness may also present itself as a symptom of degenerative diseases of the eye, such as cataract and age-related macular degeneration, and as part of the retinal damage caused by diabetes. Vitamin A deficiency may also cause color blindness. [47] Color blindness may be a side effect of prescription drug use.
The second most common PIP color vision standard is the HRR color test (developed by Hardy, Rand, and Rittler), which solves many of the criticisms of the Ishihara test. For example, it detects blue-yellow color blindness, is less susceptible to memorization and uses shapes, so it is accessible to the illiterate and young children. [2]
4-Nitroaniline, p-nitroaniline or 1-amino-4-nitrobenzene is an organic compound with the formula C 6 H 6 N 2 O 2. A yellow solid, it is one of three isomers of nitroaniline. It is an intermediate in the production of dyes, antioxidants, pharmaceuticals, gasoline, gum inhibitors, poultry medicines, and as a corrosion inhibitor. [3]
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Color blindness (or color vision deficiency) is a defect of normal color vision. Because color blindness is a symptom of several genetic and acquired conditions, the severity can range drastically from monochromacy (no color vision) to anomalous trichromacy (can be as mild as being indistinguishable from normal color vision). Congenital ...
Normalized responsivity spectra of human cone cells, S, M, and L types (SMJ data based on Stiles and Burch [1] RGB color-matching, linear scale, weighted for equal energy) [2] LMS (long, medium, short), is a color space which represents the response of the three types of cones of the human eye , named for their responsivity (sensitivity) peaks ...
The commonly used Ishihara test is used to detect mainly congenital red-green color blindness, but its usefulness is limited in detecting acquired color vision deficiencies. [3] But City University test contains test plates that can be used to detect all types of color vision deficiencies. [ 4 ]
Blue cone monochromacy (BCM) is an inherited eye disease that causes severe color blindness, poor visual acuity, nystagmus, hemeralopia, and photophobia due to the absence of functional red (L) and green (M) cone photoreceptor cells in the retina. BCM is a recessive X-linked disease and almost exclusively affects XY karyotypes.
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