Fibrinogen Baltimore III: congenital dysfibrinogenemia with a shortened gamma-subunit

Thromb Res. 1988 Aug 1;51(3):251-8. doi: 10.1016/0049-3848(88)90102-8.

Abstract

An abnormal fibrinogen has been found in an asymptomatic Negro female. Clinical laboratory findings were normal, except for a prolonged thrombin time which was corrected by addition of calcium. Fibrinopeptide release by thrombin and crosslinking by factor XIII also occurred normally, but fibrin monomer polymerization was delayed. Sodium dodecylsulfate-polyacrylamide gel electrophoresis disclosed that 50% of the gamma-subunits migrated with an apparent Mr of 45,500, approximately 1,500 Da smaller than normal. The evidence suggests that an internal sequence of 10-15 residues is missing from the gamma-subunit of the abnormal fibrinogen.

Publication types

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

MeSH terms

  • Adult
  • Blood Protein Disorders / congenital*
  • Female
  • Fibrinogens, Abnormal / isolation & purification*
  • Humans
  • Thrombin Time

Substances

  • Fibrinogens, Abnormal
  • fibrinogen Baltimore III