Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha-2-antiplasmin deficiency

Br J Haematol. 2019 Sep;186(6):e198-e201. doi: 10.1111/bjh.16077. Epub 2019 Jul 8.
No abstract available

Keywords: SERPINF2; alpha-2-antiplasmin; bleeding disorder; fibrinolytic abnormality.

Publication types

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

MeSH terms

  • Adolescent
  • Blood Coagulation Disorders, Inherited* / blood
  • Blood Coagulation Disorders, Inherited* / genetics
  • Blood Platelets / metabolism*
  • Fibrinolysis / genetics*
  • Gene Deletion*
  • Hemorrhage* / blood
  • Hemorrhage* / genetics
  • Humans
  • Male
  • Thrombelastography
  • alpha-2-Antiplasmin / deficiency*

Substances

  • SERPINF2 protein, human
  • alpha-2-Antiplasmin