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The disorder can cause heart abnormalities and seizures if the amount of methemoglobin in the blood exceeds 20 percent, but at levels between 10 and 20 percent it can cause blue skin without other symptoms. Most of the Fugates lived long and healthy lives. The "bluest" of the blue Fugates, Luna Stacy, had 13 children and lived to age 84. [6]
Mongolian spot is a congenital developmental condition—that is, one existing from birth—exclusively involving the skin.The blue colour is caused by melanocytes, melanin-containing cells, that are usually located in the surface of the skin (the epidermis), but are in the deeper region (the dermis) in the location of the spot. [6]
Paul Karason (November 14, 1950 – September 23, 2013) was an American from Bellingham, Washington, whose skin was a purple-blue color. [1]Karason was fair skinned and freckled until the early 1990s.
Oprah Winfrey is a household name,but it turns out "Oprah" is not her real name. A little known fact about the 61-year-old media mogul -- her family wanted to give her a Biblical name, so they ...
Cyanosis is the change of body tissue color to a bluish-purple hue, as a result of decrease in the amount of oxygen bound to the hemoglobin in the red blood cells of the capillary bed. [1] Cyanosis is apparent usually in the body tissues covered with thin skin, including the mucous membranes, lips, nail beds, and ear lobes. [1]
In the 2000 US Census, "White" refers to "person having origins in any of the original peoples of Europe, the Middle East, or North Africa." [21] In the 2000 US Census, "Black or African American" refers to a "person having origins in any of the Black racial groups of Africa." [21] The other three self-designated races are not labeled by color ...
The most common color is blue, although they can be blue-gray, blue-black or even deep brown. The Mongolian spot is a congenital developmental condition exclusively involving the skin . The blue colour is caused by melanocytes , melanin -containing cells, that are deep under the skin. [ 6 ]
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.