Rare coagulation deficiencies

F. Peyvandi, S. Duga, S. Akhavan, P. M. Mannucci

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)308-321
Number of pages14
JournalHaemophilia
Volume8
Issue number3
DOIs
Publication statusPublished - May 2002

Keywords

  • Afibrinogenaemia
  • Autosomal recessive disorders
  • Factor VIII
  • Factor XI
  • Factor XIII

ASJC Scopus subject areas

  • Hematology

Fingerprint Dive into the research topics of 'Rare coagulation deficiencies'. Together they form a unique fingerprint.

Cite this