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Hyperlipoproteinemia type i
(Apolipoprotein C-II Deficiency; Hyperchylomicronemia, Familial; Lipoprotein Lipase Deficiency, Familial)
An inherited condition due to a deficiency of either lipoprotein lipase or apolipoprotein c-ii (a lipase-activating protein). The lack of lipase activities results in inability to remove chylomicrons and triglycerides from the blood which has a creamy top layer after standing.
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 (hyperlipoproteinemia type www.cmaj.ca |  Hyperlipoproteinemia, type III www.gfmer.ch |  Hyperlipoproteinemia Type www.lookfordiagnosis.com |  Hyperlipoproteinemia type IA eyepathologist.com |
What is Hyperlipoproteinemia Type I? www.medify.com | View All Top Treatments for Hyperlipoproteinemia Type I → www.medify.com |  with hyperlipoproteinemia eyepathologist.com |  hyperlipoproteinemia type link.springer.com |
Diagnosis and therapies
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Wikipedia
Hyperlipidemia, Lipoprotein lipase deficiency, Medication-induced hyperlipoproteinemia, Lysosomal Acid Lipase Deficiency, French Canadian American, LPL, Lysosomal lipase, LPL Financial, Héctor Terán Terán, Péter Tímár
More information
- Reported cases - Summary of cases reported on this disease.
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