Double heterozygous mutations Gln100Leu and His348Gln of the F7 gene in a patient with factor VII deficiency

Blood Coagul Fibrinolysis. 2013 Mar;24(2):199-201. doi: 10.1097/MBC.0b013e3283551132.

Abstract

A 25-year-old Chinese woman who had a history of easy bruising was admitted to hospital due to uncontrolled epistaxis. She showed factor VII activity level of 2% and factor VII antigen level of 4% of the normal value. We detected a novel missense mutation g.8355 A>T (p.Gln100Leu) in the second epidermal growth factor-like (EGF) domain and a g.11482 T>G (p.His348Gln) in the catalytic domain. Although the Gln100 residue is close to the junction of EGF-2 domain with the serine protease domain, we infer that the substitution of polar negatively charged Gln residue at the position 100 with introduction of nonpolar Leu residue may be likely to perturb proper folding, resulting in decreasing factor VII activity.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Factor VII / genetics*
  • Factor VII / metabolism
  • Factor VII Deficiency / genetics*
  • Female
  • Heterozygote
  • Humans
  • Mutation*

Substances

  • Factor VII