The familial chylomicronemia syndrome.


The chylomicronemia syndrome is a disorder characterized by severe hypertriglyceridemia and fasting chylomicronemia. Genetic causes of the syndrome are rare and include deficiency of lipoprotein lipase (LPL), apolipoprotein C-II, and familial inhibitor of LPL. Patients with familial forms of hypertriglyceridemia in combination with secondary acquired disorders account for most individuals presenting with chylomicronemia. The clinical manifestations--lipid and other biochemical abnormalities--as well as treatment options for chylomicronemic patients are discussed.

Written by Santamarina-Fojo S., published over 4 years ago.

View the free, full text article here

Endocrinol Metab Clin North Am. 1998 Sep;27(3):551-67, viii. The familial chylomicronemia syndrome. Santamarina-Fojo S. Source: Section of Molecular Biology, Molecular Disease Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.

Written by Santamarina-Fojo S., published over 4 years ago.

No comment for «The familial chylomicronemia syndrome.»

Expand all ]

No comment yet.

Leave a comment

You must be registered and signed in to leave a comment. Sign in now.