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  • lipodystrophy
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  • membranous lipodystrophy
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  • lipodystrophy
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  • membranous lipodystrophy
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  • generalized lipodystrophy
    Àü½Å¼º Áö¹æÀÌ¿µ¾çÁõ
  • progressive lipodystrophy
    ÁøÇ༺ Áö¹æÀÌ¿µ¾çÁõ.
  • progressive lipodystrophy
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  • lipodystrophy, lipodystrophia ³ª
    Áö¹æÀÌ¿µ¾çÁõ(ò·Û¸ì¶ç½å×ñø)
  • lipodystrophy, partial
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  • centrifugal lipodystrophy
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  • dystrophy (intestinal lipodystrophy)
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  • generalized lipodystrophy
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  • insulin lipodystrophy
    Àν¶¸°Áö¹æÀÌ¿µ¾çÁõ.
  • intestinal lipodystrophy =Whipple s disease
    À强Áö¹æÀÌ¿µ¾çÁõ.
  • membranous lipodystrophy = membranous lipoatrophy
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  • partial lipodystrophy
  • progressive lipodystrophy
    ÁøÇ༺ Áö¹æÀÌ¿µ¾çÁõ.
  • progressive lipodystrophy
    ÁøÇ༺ Áö¹æÀÌ¿µ¾çÁõ(òäú¼àõ ò·Û¸ì¶ç½å×ñø)
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LD labor and delivery; laboratory data; labyrinthine defect; lactate dehydrogenase; laser Doppler; lear...
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FPLD Familial partial lipodystrophy
LD Lipodystrophy
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    Lipodystrophy, NEC
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  • centrifugal lipodystrophy
    ¿ø½É Áö¹æ ÀÌ¿µ¾çÁõ
  • membranous lipodystrophy
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    µ¿ÀǾî=membranous li
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
lipodystrophy 1. <biochemistry> Any disturbance of fat metabolism.
2. A group of conditions due to defective metabolism of fat, resulting in the absence of subcutaneous fat, which may be congenital or acquired and partial or total.
Synonym: lipoatrophy, lipodystrophia.
(18 Nov 1997)
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 7 ÆäÀÌÁö: 1
partial face-sparing lipodystrophy A syndrome beginning at puberty that resembles total lipodystrophy but is inherited as an autosomal or X-linked dominant form.
(05 Mar 2000)
membranous lipodystrophy A rare metabolic disease in which bone marrow fat cells are transformed into thick convoluted PAS-staining membranes enclosing weakly osmophilic material; leads to progressive cystic resorption of limb bones and dementia with sudanophilic leukodystrophy.
(05 Mar 2000)
congenital total lipodystrophy Lipodystrophy characterised by almost complete lack of subcutaneous fat, accelerated rate of growth and skeletal development during the first 3 to 4 years of life, muscular hypertrophy, cardiac enlargement, hepatosplenomegaly, hypertrichosis, renal enlargement, hypertriglyceridemia, and hypermetabolism; both autosomal dominant and X-linked varieties exist.
(05 Mar 2000)
progressive lipodystrophy A condition characterised by a complete loss of the subcutaneous fat of the upper part of the torso, the arms, neck, and face, sometimes with an increase of fat in the tissues about and below the pelvis.
Synonym: Barraquer's disease, lipodystrophia progessiva superior, partial lipoatrophy, Simons' disease.
(05 Mar 2000)
insulin lipodystrophy Dystrophic atrophy of subcutaneous tissues in diabetics at the site of frequent injections of insulin.
Synonym: insulin lipoatrophy.
(05 Mar 2000)
intestinal lipodystrophy <gastroenterology> A rare disorder of intestinal malabsorption that occurs as the result of the intestine. Treatment is with antibiotics.
(27 Sep 1997)
familial lipodystrophy Autosomal dominant; partial lip associated with multifacial hypoplasin, retarded bone age, and hypotichosis.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 3 ÆäÀÌÁö: 1
  • Lipodystrophy - »õâ A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy.
    Synonyms : Lipodystrophies
  • Lipodystrophy, Congenital Generalized - »õâ Congenital disorders, usually autosomal recessive, characterized by severe generalized lack of ADIPOSE TISSUE, extreme INSULIN RESISTANCE, and HYPERTRIGLYCERIDEMIA.
    Synonyms : Berardinelli-Seip Congenital Lipodystrophy, Berardinelli-Seip Congenital Lipodystrophy, Type 1, Berardinelli-Seip Congenital Lipodystrophy, Type 2, Congenital Generalized Lipodystrophy, Congenital Generalized Lipodystrophy Type 1
  • Lipodystrophy, Familial Partial - »õâ Inherited conditions characterized by the partial loss of ADIPOSE TISSUE, either confined to the extremities with normal or increased fat deposits on the face, neck and trunk (type 1), or confined to the loss of SUBCUTANEOUS FAT from the limbs and trunk (type 2).
    Synonyms : Dunnigan Syndrome, Familial Partial Lipodystrophy, Familial Partial Lipodystrophy, Kobberling Type, Familial Partial Lipodystrophy, Type 1, Familial Partial Lipodystrophy, Type 2, Familial Partial Lipodystrophy, Type 3, Koberling-Dunnigan Syndrome
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lipodystrophy (lipo
Ãâó: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
lipodystrophy Defective metabolism of fat. Includes fat loss, such as wasting in the face, arms, and legs, and fat redistribution, such as fat accumulation in the upper back or trunk.
Ãâó: www.amfar.org/cgi-bin/iowa/bridge.html
lipodystrophy a disturbance of fat METABOLISM that involves the absence of fat and/or the abnormal distribution of fat in the body. Currently, "lipodystrophy" is not clearly defined and the term is used to refer to a variety of SYNDROMES, including wasting in the face and extremities, an accumulation of abdominal fat and breast enlargement. The cause is unknown, but it could be a result of HIV infection and/or ANTIRETROVIRAL therapy.
Ãâó: www.gmhc.org/health/glossary3.html
lipodystrophy the umbrella term for pronounced loss or gain of body and blood fat that mostly afflicts HIV patients and people with rare inherited disorders.
Ãâó: cas.umkc.edu/psyc/motiv8/glossary.htm
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