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Endocrinology. Lipodystrophy syndromes are a group of genetic or acquired disorders in which the body is unable to produce and maintain healthy fat tissue. [1][2] The medical condition is characterized by abnormal or degenerative conditions of the body's adipose tissue. A more specific term, lipoatrophy (from Greek lipo 'fat' and dystrophy ...
Some had a thin sheet of bronze on the outer face, often just around the rim. The convention was to decorate the shield. The aspis measured at least 0.9 metres (2 ft 11 in) in diameter and weighed about 7.3 kilograms (16 lb), and it was about 25–38 millimetres (0.98–1.50 in) thick. [2]
Acquired generalized lipodystrophy (AGL), also known as Lawrence syndrome[1] and Lawrence–Seip syndrome, [1] is a rare skin condition that appears during childhood or adolescence, characterized by fat loss affecting large areas of the body, particularly the face, arms, and legs. [2]: 496 There are four types of lipodystrophy based on its ...
Lipoatrophy is the term describing the localized loss of fat tissue. This may occur as a result of subcutaneous injections of insulin in the treatment of diabetes, from the use of human growth hormone or from subcutaneous injections of copaxone used for the treatment of multiple sclerosis. In the latter case, an injection may produce a small ...
The Hippocratic facies (Latin: facies Hippocratica) [1] is the change produced in the face recognisable as a medical sign known as facies and prognostic of death. It may also be seen as due to long illness, excessive defecation, or excessive hunger, when it can be differentiated from the sign of impending death. (The term typhoid facies refers ...
Melanoacanthoma (pigmented seborrheic keratosis) Merkel cell carcinoma (cutaneous apudoma, primary neuroendocrine carcinoma of the skin, primary small cell carcinoma of the skin, trabecular carcinoma of the skin) Microcystic adnexal carcinoma (sclerosing sweat duct carcinoma) Micronodular basal cell carcinoma.
Congenital generalized lipodystrophy (also known as Berardinelli–Seip lipodystrophy) is an extremely rare autosomal recessive condition, characterized by an extreme scarcity of fat in the subcutaneous tissues. [2] It is a type of lipodystrophy disorder where the magnitude of fat loss determines the severity of metabolic complications. [3]
Myrtis is the name given by archaeologists to an 11-year-old girl from ancient Athens, whose remains were discovered in 1994–95 in a mass grave during work to build the metro station at Kerameikos, Greece. [1] The name was chosen from common ancient Greek names. [2] The analysis showed that Myrtis and two other bodies in the mass grave had ...