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Hypertriglyceridemia 2
- ... in women, and complications such as diabetes and hypertriglyceridemia occur more commonly in women. Familial partial lipodystrophy can be caused by mutations in several genes. Type 2 results from mutations in the LMNA gene. The ...
- ... of fats called triglycerides circulating in the bloodstream (hypertriglyceridemia) and diabetes mellitus, which is a condition in which glucose levels can become dangerously high. In some cases, congenital generalized lipodystrophy type 2 is also associated with mild to moderate intellectual ...
- ... face and upper body. Affected individuals also have hypertriglyceridemia and ... is produced within cells.Two other mutations in the CAV1 gene have been ...
- ... elevated amount of fat in the blood (mild hypertriglyceridemia); disturbances in ... Tangier disease is a rare disorder, with ...
- ... Burger-Grutz syndrome Endogenous hypertriglyceridaemia Familial fat-induced hypertriglyceridemia Familial hyperchylomicronemia Familial LPL deficiency Hyperlipoproteinemia type I ...
- ... high levels of triglycerides circulating in the bloodstream (hypertriglyceridemia) and diabetes mellitus.The AGPAT2 gene mutations that ... acyltransferase beta 1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta) 1-AGP acyltransferase 2 ...
- ... of fats called triglycerides circulating in the bloodstream (hypertriglyceridemia), which can lead to the development of small ... of the arms and legs after puberty. Type 2 can be associated with intellectual disability, which is ...