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Diseases

Genetic and Rare Diseases Information Center (GARD)

Hyperlipoproteinemia type 1


Other Names for this Disease
  • Hyperlipoproteinemia type I
  • Lipoprotein lipase deficiency
  • LPL deficiency
  • Lipase D deficiency
  • Hyperchylomicro-nemia familial
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Treatment

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What is the treatment for hyperlipoproteinemia type 1?

Treatment for hyperlipoproteinemia type 1 is intended to control blood triglyceride levels with a very low-fat diet. Fat intake usually must be less than 20 grams per day to prevent symptoms. Medium-chain fatty acids (such as coconut oil) can be incorporated into the diet, as they are absorbed by the body in a different manner. Dietary counseling may be helpful to maintain adequate calorie and nutrient intake.[1]
Last updated: 8/24/2009

References
  1. Brunzell JD. Familial Lipoprotein Lipase Deficiency. Gene Reviews. July 28, 2009; http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lpl. Accessed 8/24/2009.


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Management Guidelines

  • GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.

Clinical Trials & Research for this Disease

  • ClinicalTrials.gov lists trials that are studying or have studied Hyperlipoproteinemia type 1. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.
  • Orphanet lists European clinical trials, research studies, and patient registries enrolling people with this condition. 
Other Names for this Disease
  • Hyperlipoproteinemia type I
  • Lipoprotein lipase deficiency
  • LPL deficiency
  • Lipase D deficiency
  • Hyperchylomicro-nemia familial
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.