Please use this identifier to cite or link to this item: http://imsear.hellis.org/handle/123456789/82581
Title: Familial chylomicronemia syndrome.
Authors: Mohandas, M K
Jemila, J
Ajith Krishnan, A S
George, T Thomas
Issue Date: 11-Feb-2005
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.
URI: http://imsear.hellis.org/handle/123456789/82581
Appears in Collections:Indian Journal of Pediatrics

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