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Results 1 - 7 of 7 for Familial partial lipodystrophy
  1. Familial partial lipodystrophy is a rare condition characterized by an abnormal distribution of fatty (adipose) tissue. Adipose tissue is normally found in many ...
  2. ... the LMNA gene have been found to cause familial partial lipodystrophy type 2 (also known as familial partial lipodystrophy, Dunnigan type), a rare condition characterized by an ...
  3. Diabetes (National Library of Medicine)  
    Diabetes is a disease in which your blood glucose, or blood sugar, levels are too high. Glucose comes from the foods you eat. Insulin is a hormone that helps ...
  4. ... VIP21 Tests of CAV1 PubMed CAVEOLIN 1; CAV1 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 7; FPLD7 NCBI Gene ClinVar Boscher C, Nabi IR. Caveolin-1: role in cell signaling. Adv Exp Med Biol. 2012;729:29-50. ... partial lipodystrophy and hypertriglyceridemia. Lipids Health Dis. 2008 Jan 31; ...
  5. ... with no history of the disorder in their family. In other cases, an affected person inherits the mutation from one affected parent. Growth retardation-Rieger anomaly Lipodystrophy, partial, with Rieger anomaly and short stature Short stature- ...
  6. ... people with dense deposit disease may have acquired partial lipodystrophy, a condition characterized by a lack of fatty ( ... can occur with dense deposit disease, including acquired partial lipodystrophy and a buildup of drusen in the retina. ...
  7. ... autoinflammatory disorder showing pernio-like rashes and progressive partial lipodystrophy. Allergol Int. 2012 Jun;61(2):197-206. ...