AllRefer Health - Chylomicronemia Syndrome (Familial Lipoprotein Lipase Deficiency)

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You are here : AllRefer.com > Health > Diseases & Conditions > Chylomicronemia Syndrome

Chylomicronemia Syndrome


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•	Overview, Causes, & Risk Factors
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Alternate Names : Familial Lipoprotein Lipase Deficiency

Definition

Chylomicronemia syndrome is an inherited disorder in which abnormal lipid (fat) metabolism causes chylomicrons (a type of lipids) to accumulate to massive levels in the blood.

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Hepatomegaly

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Overview, Causes, & Risk Factors

Chylomicronemia syndrome results from impaired or absent lipoprotein lipase (LPL), an enzyme in fat and muscle responsible for the breakdown of certain lipids. In addition to Familial Lipoprotein Lipase Deficiency, a large accumulation of chylomicrons may also be seen in people with Familial Apoprotein CII Deficiency.

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• Definition
• Overview, Causes, & Risk Factors
• Symptoms & Signs
• Prevention
• Diagnosis & Tests
• Treatment
• Prognosis
• Complications
• Calling Your Health Care Provider
• Pictures & Images

Review Date : 8/18/2003
Reviewed By : David Webner, M.D., Sports Medicine Fellow, Crozer-Keystone Family Practice Program, Springfield, PA. Review provided by VeriMed Healthcare Network.

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