congenital generalized lipodystrophy

congenital generalized lipodystrophy
congenital progressive lipodystrophy total l.

Medical dictionary. 2011.

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  • Congenital generalized lipodystrophy — Classification and external resources eMedicine article/1113171 Congenital generalized lipodystrophy (also known as Berardinelli–Seip syndrome) is a rare autosomal dominant skin condition, characterized by an extreme paucity of fat in the… …   Wikipedia

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  • Lipodystrophy — A disorder of adipose (fatty) tissue characterized by a selective loss of body fat. Patients with lipodystrophy have a tendency to develop insulin resistance, diabetes, a high triglyceride level (hypertriglyceridemia), and fatty liver. There are… …   Medical dictionary

  • Centrifugal abdominal lipodystrophy — (also known as Centrifugal lipodystrophy, [1] Lipodystrophia centrifugalis abdominalis infantalis [1]) is a skin condition characterized by areas of subcutaneous fat loss that slowly enlarge.[2]:496 7 See also Lipodystrophy List of cutaneous… …   Wikipedia

  • lipodystrophy — n. any condition resulting in the loss and/or redistribution of fat tissue in part or all of the body. It may be congenital or acquired later in life (for example, as an adverse effect of drug treatment). Congenital lipodystrophies include… …   The new mediacal dictionary

  • total lipodystrophy — a rare, autosomal recessive disorder seen mainly in infant girls, characterized by generalized loss of subcutaneous and extracutaneous adipose tissue with hepatomegaly, hypoglycemia and insulin resistant nonketotic diabetes, hyperlipemia,… …   Medical dictionary

  • List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… …   Wikipedia

  • AGPAT2 — 1 acylglycerol 3 phosphate O acyltransferase 2 (lysophosphatidic acid acyltransferase, beta), also known as AGPAT2, is a human gene.cite web | title = Entrez Gene: AGPAT2 1 acylglycerol 3 phosphate O acyltransferase 2 (lysophosphatidic acid… …   Wikipedia

  • Barraquer–Simons syndrome — Barraquer Simons syndrome Classification and external resources ICD 10 272.6 OMIM 608709 DiseasesDB …   Wikipedia

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