Editorial commentary: Dietary management of familial chylomicronemia syndrome

J Clin Lipidol. 2016 May-Jun;10(3):462-5. doi: 10.1016/j.jacl.2015.12.023. Epub 2016 Jan 7.

Authors

Lauren Williams¹, Don P Wilson²

Affiliations

¹ Cardiovascular Health and Risk Reduction Program, Cook Children's Medical Center, Fort Worth, TX, USA. Electronic address: lauren.williams2@cookchildrens.org.
² Cardiovascular Health and Risk Reduction Program, Cook Children's Medical Center, Fort Worth, TX, USA.

PMID: 27206931
DOI: 10.1016/j.jacl.2015.12.023

No abstract available

Keywords: Familial chylomicronemia syndrome; Hypertriglyceridemia; Lipoprotein lipase deficiency; Medical nutritional therapy.

Publication types

Editorial
Research Support, Non-U.S. Gov't

MeSH terms

Apolipoproteins C / deficiency
Apolipoproteins C / genetics
Chylomicrons / blood
Chylomicrons / genetics
Diet, Fat-Restricted*
Humans
Hyperlipoproteinemia Type I / diet therapy*
Hypertriglyceridemia / diet therapy*
Hypertriglyceridemia / genetics
Lipoprotein Lipase / deficiency
Lipoprotein Lipase / genetics
Mutation

Substances

Apolipoproteins C
Chylomicrons
Lipoprotein Lipase