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Familial hypertriglyceridemia : ウィキペディア英語版 | Familial hypertriglyceridemia Familial hypertriglyceridemia is an autosomal dominant condition occurring in approximately 1% of the population.〔Boman H,Hazzard WR, AlbersJJ, et ah Frequency of monogenic forms of hyperlipidemia in a normal population. AmJ ttum Genet 27:19A,1975. ()〕 Triglyceride levels, but not cholesterol, are elevated as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. Unlike familial hypercholesterolemia, there is no association with premature coronary disease. However, affected individuals are at risk for chylomicronemia syndrome, characterized by elevated chylomicrons in the blood. == See also ==
* Primary hyperlipoproteinemia * Familial apoprotein CII deficiency * Skin lesion
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Familial hypertriglyceridemia」の詳細全文を読む
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