This site is intended for healthcare professionals
Journals
  • Home
  • /
  • Journals
  • /
  • Coagulation and haemorrhagic disorders
  • /
  • Bleeding and thrombosis in 55 patients with inheri...
Journal

Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia.

Read time: 1 mins
Published:30th Sep 1999
Author: Lak M, Keihani M, Elahi F, Peyvandi F, Mannucci PM.
Availability: Pay for access, or by subscription
Ref.:Br J Haematol. 1999;107(1):204-6.
DOI:10.1046/j.1365-2141.1999.01681.x

Knowledge of the spectrum of symptoms in patients with inherited afibrinogenaemia is limited by the rarity of this coagulation defect. We compared a large series of 55 afibrinogenaemic patients from Iran with 100 patients with severe factor VIII deficiency. In afibrinogenaemia there was a higher frequency of mucosal?type bleeding symptoms but joint and muscle bleeding was less frequent and severe than in haemophilia. Umbilical cord bleeding was relatively frequent only in afibrinogenaemic patients.

Two young patients developed spontaneous thrombotic episodes and three women had recurrent abortions. Overall, in afibrinogenaemia bleeding symptoms are qualitatively different and less severe than in haemophilia. Afibrinogenaemia can also be accompanied by thrombotic manifestations.

 

Read abstract on library site

Access full article