familial combined hyperlipidemia


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familial combined hyperlipidemia

Metabolic disease A common–1:300 AD disorder with ↑ TGs and/or cholesterol Lab ↑ apoB, ↑ LDL-C, ↑ VLDL-C, mild ↓ HDL-C, apoA1 Clinical CAD, first MI as early as age 40, overweight, HTN Management Diet–weight loss, exercise, lipid-lowering drugs; smoking is forbidden as it exacerbates ASHD
References in periodicals archive ?
Relationship of insulin sensitivity and apoB levels to intrabdominal fat in subjects with familial combined hyperlipidemia.
Association of the apolipoprotein A1/C3/A4/A5 gene cluster with triglyceride levels and LDL particle size in familial combined hyperlipidemia.
Impaired chylomicron remnant clearance in familial combined hyperlipidemia.
Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia.
Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia.
Genetics and molecular biology of familial combined hyperlipidemia.

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