FH Tulsa-1 and -2: two unique alleles for familial hypercholesterolemia presenting in an affected two-year-old African-American male

Am J Med Genet. 1995 Nov 20;59(3):300-3. doi: 10.1002/ajmg.1320590307.

Abstract

A two-year-old African American boy presented with cutaneous xanthomata and extreme hypercholesterolemia. Subsequent studies revealed that the LDL-cholesterol was 1,001 mg/dl and apoB 507 mg/dl. LDL-receptor activity was almost undetectable, which is compatible with the finding of two newly described defective alleles on exon 4 of the LDL-receptor gene coding for part of the ligand-binding domain. One allele contained a 21 base-pair insertion from codon 200 to 207 whereas the other had a point mutation at codon 207. The rarity of genes for FH reported in individuals of African ancestry is discussed.

Publication types

  • Case Reports

MeSH terms

  • Alleles*
  • Base Sequence
  • Black People / genetics
  • Child, Preschool
  • Codon / genetics
  • Exons / genetics
  • Female
  • Humans
  • Hyperlipoproteinemia Type II / blood
  • Hyperlipoproteinemia Type II / complications
  • Hyperlipoproteinemia Type II / ethnology
  • Hyperlipoproteinemia Type II / genetics*
  • Lipids / blood
  • Male
  • Molecular Sequence Data
  • Point Mutation
  • Receptors, LDL / genetics*
  • Xanthomatosis / etiology*

Substances

  • Codon
  • Lipids
  • Receptors, LDL