Rare coagulation deficiencies

Haemophilia. 2002 May;8(3):308-21. doi: 10.1046/j.1365-2516.2002.00633.x.


Deficiencies of coagulation factors (other than factor VIII and factor IX) that cause a bleeding disorder are inherited as autosomal recessive traits and are generally rare, with prevalences in the general population varying between 1 : 500 000 and 1 : 2 000 000. In the last few years, the number of patients with recessively transmitted coagulation deficiencies has increased in European countries with a high rate of immigration of Islamic populations, because in these populations, consanguineous marriages are frequent. Owing to the relative rarity of these deficiencies, the type and severity of bleeding symptoms, the underlying molecular defects and the actual management of bleeding episodes are not as well established as for haemophilia A and B. This article reviews these disorders in terms of their clinical manifestations and characterization of the molecular defects involved. The general principles of management are also discussed.

Keywords: afibrinogenaemia, autosomal recessive disorders, factor VIII, factor XI, factor XIII.

Publication types

  • Review

MeSH terms

  • Blood Coagulation Factors / genetics
  • Blood Coagulation Factors / therapeutic use
  • Coagulation Protein Disorders / diagnosis
  • Coagulation Protein Disorders / etiology
  • Coagulation Protein Disorders / genetics*
  • Genes, Recessive
  • Hemophilia A
  • Humans
  • Mutation


  • Blood Coagulation Factors