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Ency. home > Disease > C > Chylomicronemia syndrome

Chylomicronemia syndrome   

Overview | Symptoms | Treatment | Prevention

Alternative names:

Familial Lipoprotein Lipase Deficiency

Definition:

An inherited disorder associated with abnormal lipid (fat) metabolism in which chylomicrons (a type of lipids) accumulate to massive levels in the plasma.

Causes and Risks

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.

Ency. home > Disease > C > Chylomicronemia syndrome

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