Canadian Medical Guide > Diseases > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Lipoprotein Lipase Deficiency, Familial Terms and Definitions




Lipoprotein Lipase Deficiency, Familial

Medical Definition: A rare familial condition characterized by massive chylomicronemia and decreased levels of other lipoproteins. It is due to deficiency of lipoprotein lipase, an alkaline triglyceride hydrolase which catalyzes an important step in the extrahepatic removal of triglyceride-rich lipoproteins from the blood.
Guide Notes: do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Previously Indexed: Hyperlipidemia/familial & genetic (1966-1979)

Lipoprotein Lipase Deficiency, Familial Medical Definitions and Terms

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