1.
Indian J Pediatr
; 2005 Feb; 72(2): 181
Artículo
en Inglés
| IMSEAR
| ID: sea-82581
RESUMEN
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.