[Factor XI deficiency caused by a mutation of Gly400Val]

Rinsho Ketsueki. 2007 Feb;48(2):148-50.
[Article in Japanese]

Abstract

The patient described herein is a 69-year-old Japanese woman with a history of excessive bleeding after left heminephrectomy for a malignant renal tumor at 31 years of age. Her parents, who do not have abnormal bleeding, are first cousins. Her factor XI activity was less than 1% of normal with an prolonged activated partial thromboplastin time (APTT) of 74.3 seconds. Analysis of the patient's factor XI genes revealed homozygosity for a valine substituting for the wild-type glycine at amino acid 400 (Gly400Val). The patient has two children, neither of whom has abnormal bleeding and whose factor XI activities are 62% and 57% of normal, with APTT levels within normal limits in both cases. We herein report on a Japanese family with factor XI deficiency caused by Gly400Val mutation.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Aged
  • Amino Acid Substitution / genetics*
  • Codon / genetics
  • DNA / genetics
  • Exons / genetics
  • Factor XI / genetics*
  • Factor XI Deficiency / genetics*
  • Female
  • Glycine*
  • Homozygote
  • Humans
  • Mutation, Missense*
  • Valine*

Substances

  • Codon
  • DNA
  • Factor XI
  • Valine
  • Glycine