A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene

Thromb Haemost. 2000 Jul;84(1):49-53.


Congenital afibrinogenemia due to a novel homozygous nonsense mutation of the fibrinogen gamma-chain gene, fibrinogen Hakata, was found in an 18-year-old Japanese girl who had received supplemental fibrinogen therapy since she was 4 months old. The plasma fibrinogen concentrations of the proband were measured as less than 10 mg/dl by a functional method and less than 17 mg/dl by an immunological method. Fibrinogen concentrations of her family were in the range of 94-164 mg/dl. The proband and her family had no other clinical symptoms. Genomic DNA of the proband and her family was isolated from leukocytes, and all exons of fibrinogen subunits and their intron/exon boundaries were analyzed. A genetic mutation, a guanine-to-thymine (G-to-T) transversion at the nucleotide position of 5860, was identified on exon 7 of the gamma-chain gene. This mutation changed the codon for the 231st residue of the gamma-chain from GAG (Glu) to TAG (stop). No other mutation was observed. Aalpha, Bbeta and gamma chains were observed in plasma of the heterozygous family members. However, only a trace amount of Aalpha chain and no gamma chain was detected in the plasma of the proband.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afibrinogenemia / blood
  • Afibrinogenemia / genetics*
  • Base Sequence
  • Blood Protein Electrophoresis
  • Codon / genetics
  • Codon, Nonsense*
  • Codon, Terminator
  • Female
  • Fibrinogens, Abnormal / chemistry
  • Fibrinogens, Abnormal / genetics*
  • Fibrinogens, Abnormal / isolation & purification
  • Humans
  • Infant, Newborn
  • Male
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Protein Subunits


  • Codon
  • Codon, Nonsense
  • Codon, Terminator
  • Fibrinogens, Abnormal
  • Protein Subunits
  • fibrinogen Hakata