Familial defective apolipoprotein B-100: molecular basis, prevalence and clinical features

Wien Klin Wochenschr. 1991;103(20):621-5.

Abstract

Familial defective apo B-100 is an autosomal dominant trait which causes moderate to severe elevation of LDL-cholesterol in the plasma and may predispose the coronary heart disease. The primary defect is a single amino acid change (Arg3500 to Gln), which disrupts the normal binding of LDL to the LDL-receptor. The mutation occurs at an estimated frequency of 1/600 in the normal population and is, therefore one of the most common known single-gene defects causing an inherited abnormality.

Publication types

  • Review

MeSH terms

  • Alleles
  • Apolipoprotein B-100
  • Apolipoproteins B / blood
  • Apolipoproteins B / genetics*
  • Cholesterol, LDL / blood
  • Cholesterol, LDL / genetics*
  • Gene Frequency / genetics
  • Humans
  • Hyperlipoproteinemia Type II / blood
  • Hyperlipoproteinemia Type II / genetics*
  • Pedigree
  • Risk Factors

Substances

  • Apolipoprotein B-100
  • Apolipoproteins B
  • Cholesterol, LDL