Familial chylomicronemia syndrome: a novel mutation in the lipoprotein lipase gene

Acta Gastroenterol Belg. 2024 Apr-Jun;87(2):326-328. doi: 10.51821/87.2.12025.
No abstract available

Keywords: child; chylomicronemia; hyper-triglyceridemia; lipoprotein lipase; pancreatitis.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Female
  • Humans
  • Hyperlipoproteinemia Type I* / diagnosis
  • Hyperlipoproteinemia Type I* / genetics
  • Lipoprotein Lipase* / genetics
  • Male
  • Mutation*

Substances

  • Lipoprotein Lipase

Supplementary concepts

  • Familial hyperchylomicronemia syndrome