A family with complete deficiency of plasma cholesteryl ester transfer protein activities

Intern Med. 1994 Jul;33(7):432-6. doi: 10.2169/internalmedicine.33.432.

Abstract

A 43-year-old male with a high value of high density lipoprotein cholesterol (151 mg/dl) was found among subjects receiving annual health checks. We investigated the cholesteryl ester transfer protein (CETP) activity and conducted a family study. There was complete deficiency of CETP activities in the proband and his sister, and partial deficiency of CETP activities in his mother and daughter. Genetic analysis revealed a splicing defect (G to A point mutation) in intron 14 of the CETP gene.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Apolipoproteins / blood*
  • Carrier Proteins / blood*
  • Carrier Proteins / genetics
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL / blood*
  • DNA / genetics
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Genotype
  • Glycoproteins*
  • Humans
  • Lipids / blood*
  • Male
  • Pedigree
  • Point Mutation

Substances

  • Apolipoproteins
  • CETP protein, human
  • Carrier Proteins
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Glycoproteins
  • Lipids
  • DNA