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|Title:||Familial chylomicronemia syndrome.|
|Authors:||Mohandas, M K|
Ajith Krishnan, A S
George, T Thomas
|Citation:||Mohandas MK, Jemila J, Ajith Krishnan AS, George TT. Familial chylomicronemia syndrome. Indian Journal of Pediatrics. 2005 Feb; 72(2): 181|
|Abstract:||Familial chylomicronemia syndrome is a group of rare genetic disorders characterized by deficient activity of an enzyme lipoprotein lipase or apo-protein C-II deficiency. Incidence is 1 out of 1,000,000. Alternative names to this syndrome are Type I hyper lipoproteinemia and familial lipoprotein lipase deficiency.|
|Appears in Collections:||Indian Journal of Pediatrics|
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