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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.
Publicly stated that he is unable to see mid-tones but has not specified which colors. [51] Chris Rogers: b. 1977 Australia: Cricketer: Struggles with ball color. [52] Fred Rogers: red–green 1928–2003 United States: Children's television presenter (Mister Rogers' Neighborhood) [53] [54] Roger Staubach: red–green b. 1942 United States: NFL ...
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.
Males are more likely to inherit red–green color blindness than females, because the genes for the relevant opsins are on the X chromosome. [1] Screening for congenital red–green color blindness is typically performed with the Ishihara or similar color vision test. [1] It is a lifelong condition, and has no known cure or treatment. [1]
Congenital red-green color blindness, the genetic condition that causes the most cases of color blindness. Dichromacy, a type of color vision possessed by most mammals; partial color blindness when in humans. Monochromacy, a lack of color vision; total color blindness when in humans. Achromatopsia, a syndrome that includes total color blindness.
The pointed ear(s) in Stahl's ear is caused by misshapen cartilage. It is characterized by an extra horizontal fold of cartilage (crus). Normally, there are two: superior and inferior. In Stahl's ear, there is a third horizontal crus. The helix (or upper portion of the ear) may uncurl, giving the ear a pointed shape. [10] Author Holly Black and ...
It is called preauricular sinus which, according to the U.S. National Institutes of Health, or NIH, "generally appears as a tiny skin-lined hole or pit, often just in front of the upper ear where ...
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin.