Hyperlipoproteinemia Type III
"Hyperlipoproteinemia Type III" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessively inherited disorder characterized by the accumulation of intermediate-density lipoprotein (IDL or broad-beta-lipoprotein). IDL has a CHOLESTEROL to TRIGLYCERIDES ratio greater than that of VERY-LOW-DENSITY LIPOPROTEINS. This disorder is due to mutation of APOLIPOPROTEINS E, a receptor-binding component of VLDL and CHYLOMICRONS, resulting in their reduced clearance and high plasma levels of both cholesterol and triglycerides.
|Hyperlipoproteinemia Type III
- Hyperlipoproteinemia Type III
- Dysbetalipoproteinemia, Familial
- Familial Hypercholesterolemia with Hyperlipemia
- Hyperlipoproteinemia, Broad-beta
- Broad-beta Hyperlipoproteinemia
- Hyperlipoproteinemia, Broad beta
- Hyperlipoproteinemia, Type III
- Hyperlipoproteinemias, Type III
- Type III Hyperlipoproteinemia
- Type III Hyperlipoproteinemias
- Broad Beta Disease
- Familial Dysbetalipoproteinemia
Below are MeSH descriptors whose meaning is more general than "Hyperlipoproteinemia Type III".
Below are MeSH descriptors whose meaning is more specific than "Hyperlipoproteinemia Type III".
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Below are the most recent publications written about "Hyperlipoproteinemia Type III" by people in Profiles.
Tuberous xanthomas associated with olanzapine therapy and hypertriglyceridemia in the setting of a rare apolipoprotein E mutation. Endocr Pract. 2006 Mar-Apr; 12(2):183-7.
Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia. J Biol Chem. 1991 Jun 05; 266(16):10479-84.