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Familial lipoprotein lipase deficiency |
Burger-Grutz syndrome; Hyperchylomicronemia, Familial; Hyperlipoproteinemia Type I; Lipase D deficiency; LIPD deficiency; Lipoprotein Lipase Deficiency, Familial |
Familial lipoprotein lipase deficiency is an inherited condition involving lipid metabolism (the breakdown and use of fats within the body). The condition is characterized by inflammation of the pancreas (pancreatitis), abdominal pain, and skin lesions called eruptive xanthomas.
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Familial lipoprotein lipase deficiency Other1 of 1
Familial lipoprotein lipase deficiency
... Familial lipoprotein lipase deficiency is an inherited condition involving lipid metabolism (the breakdown and use of fats within the body). The condition is characterized by inflammation of the pancr...
Source: Genetics Home Reference
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Familial lipoprotein lipase deficiency Articles
- Familial lipoprotein lipase deficiency
... Familial lipoprotein lipase deficiency is an inherited condition involving lipid metabolism (the breakdown and use of fats within the body). The condition is characterized by inflammation of the pancr...
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