Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of reported mutations: 75 % are clustered in exons 5 and 6

Ann Genet. 2001 Jan-Mar;44(1):25-32. doi: 10.1016/s0003-3995(01)01037-1.

Abstract

We have investigated the lipoprotein lipase (LPL) gene of a 2-year-old patient presenting classical features of the familial LPL deficiency including undetectable LPL activity. DNA sequence analysis of exon 5 identified the patient as a homozygote for the Gly188Glu mutation, frequently involved in this disease. A review of cases of LPL deficiency with molecular study of the LPL gene showed a total number of 221 reported mutations involved in this disease. Gly188Glu was involved in 23.5 % of cases and 74.6 % of mutations were clustered in exons 5 and 6. Based on these observations, we propose a method of screening for mutations in this gene.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Amino Acid Substitution
  • Consanguinity
  • Exons
  • Female
  • Homozygote
  • Humans
  • Hyperlipoproteinemia Type I / genetics*
  • Infant
  • Lipolysis
  • Lipoprotein Lipase / chemistry
  • Lipoprotein Lipase / deficiency*
  • Lipoprotein Lipase / genetics*
  • Male
  • Mutation, Missense*
  • Sequence Deletion

Substances

  • Lipoprotein Lipase