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Dictionary » Burger-Grutz type familial hyperchylomicronemia

Burger-Grutz type familial hyperchylomicronemia

Introduction: Burger-Grutz type familial hyperchylomicronemia

Description of Burger-Grutz type familial hyperchylomicronemia

Burger-Grutz type familial hyperchylomicronemia: 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.
Source: Diseases Database

Burger-Grutz type familial hyperchylomicronemia: Related Topics

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Source: Diseases Database

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