Chylomicronemia syndrome

Chylomicronemia syndrome
Definition
Chylomicronemia syndrome is a disorder passed down through families in which the body does not break down fats (lipids) correctly. This causes fat particles called chylomicrons to build up in the blood.

Chylomicronemia syndrome
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Chylomicronemia syndrome
Alternate Names : Familial lipoprotein lipase deficiency
Definition ...

familial chylomicronemia syndrome
medical dictionary
An inherited disorder resulting in accumulation of chylomicrons as well as triacylglycerols.

Dr. Koop - Chylomicronemia syndrome
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Discovery Health "Chylomicronemia Syndrome - Medical Dictionary" ...

Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. In: The Metabolic and Molecular Basis of Inherited Disease, 7th ed, Scriver, CR, Beaudet al, Sly, WS, Valle, D (Eds), McGraw Hill, New York, 2002.

Gene Review: Familial Lipoprotein Lipase Deficiency
Gene Test: Familial Lipoprotein Lipase Deficiency
MedlinePlus Encyclopedia: Chylomicronemia Syndrome
MedlinePlus Encyclopedia: Familial Lipoprotein Lipase Deficiency ...

See also: Familial lipoprotein lipase deficiency, Deficiency, Dystrophy, Symptom, Prevention