familial hypertriglyceridemia…

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familial hypertriglyceridemia, common inherited disorder, the concentration of very low density lipoprotein, vldl, elevated, in the plasma, leads to increased risk of heart disease, obesity, pancreatitis, this disorder, a gene mutation which is passed on in an autosomal dominant fashion, get the gene from just one of parents, have the condition, gene mutation, familial hypertriglyceridemia causes, a mild to moderate elevation of triglycerides, in the blood, though exactly how it does so, at this time, gene, genes that cause familial hypertriglyceridemia, does not, manifest, puberty, early adulthood, obesity, hyperglycemia, high blood glucose levels, high levels of insulin, frequently associated, familial hypertriglyceridemia occurs in, 1 in 300 individuals, risk factors, a family history of hypertriglyceridemia, a family history of heart disease, the age of 50, manifest, premature coronary artery disease, , mildly to moderately elevated coronary risk profile, triglycerides, elevated vldl, goal of treatment, control exacerbating conditions, obesity, hypothyroidism, diabetes wherever possible, alcohol use, discontinued, oral contraceptive use, reviewed, specific type chosen, restriction of excess calories, reduction of saturated fats, in the diet is indicated, high triglyceride levels persist, maximum dietary treatment, drug therapy, started, nicotinic acid, gemfibrozil, drugs, effectively reduced triglycerides in people affected, familial hypertriglyceridemia, there, increased risk of coronary artery disease, pancreatitis, weight loss, control of diabetes has a positive effect on the outcome, , increased risk of pancreatitis, increased risk of coronary artery disease, call health care provider, screening, family members, found to have elevated triglyceride, ldl levels, screening family members, high triglycerides, detect the disease early.