The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects

JAMA. 1991 Feb 20;265(7):904-8.

Authors

S Santamarina-Fojo¹, H B Brewer Jr

Affiliation

¹ Molecular Disease Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Md. 20892.

PMID: 1992190

No abstract available

Publication types

Case Reports
Clinical Conference

MeSH terms

Apolipoprotein C-II
Apolipoproteins C / deficiency
Apolipoproteins C / genetics
Child, Preschool
Chylomicrons / blood*
Chylomicrons / genetics
DNA / analysis
Dietary Fats / administration & dosage
Humans
Hypertriglyceridemia / drug therapy
Hypertriglyceridemia / genetics*
Hypertriglyceridemia / pathology
Lipoprotein Lipase / genetics
Male
Pancreatitis / genetics
Pancreatitis / pathology
Polymerase Chain Reaction
Syndrome

Substances

Apolipoprotein C-II
Apolipoproteins C
Chylomicrons
Dietary Fats
DNA
Lipoprotein Lipase