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Related Experiment Videos

[Primary hyperchylomicronemia and gene defects].

M Iwasaki1, N Tada

  • 1Jikei Medical University, Internal Medicine 4(Aoto).

Nihon Rinsho. Japanese Journal of Clinical Medicine
|January 19, 2000
PubMed
Summary

Primary Hyperchylomicronemia, characterized by high triglyceride levels, stems from genetic defects like lipoprotein lipase (LPL) deficiency. This summary covers gene variations and clinical symptoms of this rare disorder.

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Area of Science:

  • Genetics
  • Metabolic Disorders
  • Clinical Medicine