Hyperlipoproteinemia Type III
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Hyperlipoproteinemia Type III is not the name you expected.
Hyperlipoproteinemia type III, also known as dysbetalipoproteinemia or broad beta disease, is a rare genetic disorder characterized by improper breakdown (metabolism) of certain fatty materials known as lipids, specifically cholesterol and triglycerides. This results in the abnormal accumulation of lipids in the body (hyperlipidemia). Affected individuals may develop multiple yellowish, lipid-filled bumps (papules) or plaques on the skin (xanthomas). Affected individuals may also develop the buildup of fatty materials in the blood vessels (artherosclerosis) potentially obstructing blood flow and resulting in coronary heart disease or peripheral vascular disease. Most cases of hyperlipoproteinemia type III are inherited as an autosomal recessive trait.
American Heart Association
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Genetic and Rare Diseases (GARD) Information Center
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March of Dimes
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NIH/National Heart, Lung and Blood Institute
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For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders (NORD). For a full-text version of this report, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".
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Last Updated: 2/8/2008
Copyright 2005 National Organization for Rare Disorders, Inc.
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