Medical Definition of Familial hyperchylomicronaemia with hyperprebetalipoproteinaemia

1. Hyperlipoproteinaemia characterised by increased plasma levels of chylomicrons, VLDL, pre-beta-lipoproteins, and triglycerides, and slight rise of cholesterol on a normal diet, with beta-lipoproteins normal; may be accompanied by bouts of abdominal pain, hepatosplenomegaly, susceptibility to atherosclerosis, and abnormal glucose tolerance; probably autosomal recessive inheritance. Synonym: combined fat-and carbohydrate-induced hyperlipaemia, familial hyperchylomicronaemia with hyperprebetalipoproteinaemia, mixed hyperlipaemia. (05 Mar 2000)



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Lexicographical Neighbors of Familial Hyperchylomicronaemia With Hyperprebetalipoproteinaemia

familial dysbetalipoproteinaemia
familial emphysema
familial erythroblastic anaemia
familial fat-induced hyperlipaemia
familial glycinuria
familial goiter
familial high density lipoprotein deficiency
familial hyperbetalipoproteinaemia
familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia
familial hypercholesteraemic xanthomatosis
familial hypercholesterolaemia
familial hypercholesterolaemia with hyperlipaemia
familial hypercholesterolemia
familial hyperchylomicronaemia
familial hyperchylomicronaemia with hyperprebetalipoproteinaemia (current term)
familial hyperlipoproteinaemia
familial hyperprebetalipoproteinaemia
familial hypertriglyceridaemia
familial hypertriglyceridemia
familial hypertrophic cardiomyopathy
familial hypobetalipoproteinaemia
familial hypophosphatemic rickets
familial intestinal polyposis
familial juvenile nephrophthisis
familial lipodystrophy
familial lipoprotein lipase deficiency
familial lipoprotein lipase inhibitor

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