1.
Indian J Pediatr
;
2005 Feb; 72(2): 181
Article
in English
| IMSEAR
| ID: sea-82581
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.