Compound heterozygosity for abetalipoproteinaemia and familial hypobetalipoproteinaemia

J Med Genet. 1990 Feb;27(2):133-4. doi: 10.1136/jmg.27.2.133.

Abstract

A 10 year old boy with abetalipoproteinaemia is reported. His mother and grandfather suffered from familial hypobetalipoproteinaemia, but his father had a normal lipoprotein profile. This is the first report of abetalipoproteinaemia resulting from compound heterozygosity for abetalipoproteinaemia and familial hypobetalipoproteinaemia.

Publication types

  • Case Reports

MeSH terms

  • Abetalipoproteinemia / genetics*
  • Apolipoproteins A / blood
  • Apolipoproteins B / blood
  • Child
  • Cholesterol / blood
  • Heterozygote
  • Humans
  • Hypobetalipoproteinemias / genetics*
  • Hypolipoproteinemias / genetics*
  • Male
  • Pedigree

Substances

  • Apolipoproteins A
  • Apolipoproteins B
  • Cholesterol