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Color blindness or color vision deficiency ( CVD) is the decreased ability to see color or differences in color. [2] The severity of color blindness ranges from mostly unnoticeable to full absence of color perception. Color blindness is usually an inherited problem or variation in the functionality of one or more of the three classes of cone ...
Specialty. ophthalmology. ICD-9-CM. 95.06. MeSH. D003119. [ edit on Wikidata] The Ishihara test is a color vision test for detection of red–green color deficiencies. It was named after its designer, Shinobu Ishihara, a professor at the University of Tokyo, who first published his tests in 1917.
Dichromacy. Specialty. Ophthalmology. Dichromacy (from Greek di, meaning "two" and chromo, meaning "color") is the state of having two types of functioning photoreceptors, called cone cells, in the eyes. Organisms with dichromacy are called dichromats. Dichromats require only two primary colors to be able to represent their visible gamut.
Achromatopsia. 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.
Optic neuropathy is damage to the optic nerve from any cause. The optic nerve is a bundle of millions of fibers in the retina that sends visual signals to the brain. Damage and death of these nerve cells, or neurons, leads to characteristic features of optic neuropathy. The main symptom is loss of vision, with colors appearing subtly washed out ...
Retinopathy of prematurity ( ROP ), also called retrolental fibroplasia ( RLF) and Terry syndrome, is a disease of the eye affecting prematurely born babies generally having received neonatal intensive care, in which oxygen therapy is used because of the premature development of their lungs. [2]
1 in 40,000 newborns [1] Leber congenital amaurosis ( LCA) is a rare inherited eye disease that appears at birth or in the first few months of life. [2] It affects about 1 in 40,000 newborns. [1] LCA was first described by Theodor Leber in the 19th century. [3] [4] It should not be confused with Leber's hereditary optic neuropathy, which is a ...
Amaurosis fugax. The arteries of the choroid and iris. The greater part of the sclera has been removed. Amaurosis fugax ( Greek: ἀμαύρωσις, amaurosis meaning 'darkening', 'dark', or 'obscure', Latin: fugax meaning 'fleeting') is a painless temporary loss of vision in one or both eyes. [3]