familial hypertriglyceridemia

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1. See type I familial hyperlipoproteinemia.

2. See type IV familial hyperlipoproteinemia.

familial hypertriglyceridemia

Metabolic disease A common–1:200 AD disorder, due to ↑ in production of TGs, cholesterol, cholic acid, with ↑ VLDL and TG transport Clinical ↑ TGs, obesity, alcohol consumption, drug therapy–β-adrenergics, diuretics, estrogens, corticosteroids Management Diet, exercise, lipid-lowering drugs–eg, clofibrate, gemfibrozil

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type I familial hyperlipoproteinemia

type IV familial hyperlipoproteinemia

The hereditary types of hyperlipoproteinemia are familial lipoprotein lipase deficiency and/or apoprotein C-II deficiency (type I or V), familial hypercholesterolemia (type IIa or IIb), familial dysbetalipoproteinemia type III), familial hypertriglyceridemia (type IV), and combined hypercholesterolemia (type IIa, IIb, and/or IV) (table).

Xanthoma of the temporal bone: A unique case of this rare condition by Keane, William M. / Ear, Nose and Throat Journal

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familial hypercholesterolemia
familial hypercholesterolemia with hyperlipemia
familial hyperchylomicronemia
familial hyperchylomicronemia with hyperprebetalipoproteinemia
familial hyperglyceridemia
familial hyperlipoproteinemia
familial hyperprebetalipoproteinemia
familial hypertriglyceridemia
familial hypertrophic cardiomyopathy
familial iminoglycinuria
familial intestinal polyposis
familial intraosseous fibrous swelling of the jaws
familial juvenile nephronophthisis
familial juvenile nephrophthisis
familial lipoprotein lipase deficiency

familial histiocytic reticulosis, histiocytic medullary reticulosis
Familial histiocytosis with eosinophilia
Familial homicide
Familial Horizontal Gaze Palsy with Progressive Scoliosis
Familial Hyperaldosteronism Type I
familial hyperbetalipoproteinemia
familial hyperbetalipoproteinemia and hyperprebetalipoproteinemia
Familial hypercalcemia with nephrocalcinosis and indicanuria
Familial hypercalcemia with nephrocalcinosis and indicanuria
Familial Hypercholanemia
Familial hypercholesterolaemia
Familial hypercholesterolaemia
familial hypercholesterolemia
familial hypercholesterolemia
familial hypercholesterolemia
familial hypercholesterolemia with hyperlipemia

familial hyperchylomicronemia
familial hyperchylomicronemia with hyperprebetalipoproteinemia
familial hyperglyceridemia
Familial Hyperkalemic Periodic Paralysis
Familial Hyperkalemic Periodic Paralysis
familial hyperlipoproteinemia
familial hyperprebetalipoproteinemia
Familial Hyperreninemic Hypoaldosteronism
familial hypertriglyceridemia
familial hypertrophic cardiomyopathy
familial hypertrophic cardiomyopathy
Familial Hypoalphalipoproteinemia
Familial Hypoalphalipoproteinemia
Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia
Familial Hypocalciuric Hypercalcemia

Familial Hypokalemic Periodic Paralysis
Familial Hypokalemic Periodic Paralysis
Familial Hypokalemic Periodic Paralysis
familial hypophosphatemia
familial hypophosphatemia
familial hypophosphatemia
familial hypophosphatemic rickets
familial hypophosphatemic rickets
familial hypophosphatemic rickets
familial hypophosphatemic rickets
familial hypophosphatemic rickets
Familial Idiopathic Basal Ganglia Calcification
Familial Idiopathic Gonadotropin Deficiency
Familial Idiopathic Low-Molecular-Weight Proteinuria
Familial Idiopathic Nonarteriosclerotic Cerebral Calcification
familial iminoglycinuria

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