HELLP syndrome associated with factor V R506Q mutation.

Abstract:

:The pathogenesis of HELLP (haemolysis, elevated liver enzyme and low platelet count) syndrome, a severe presentation of pre-eclampsia, is still an enigma. Activated protein C resistance resulting from a mutation in coagulation factor V has recently emerged as the leading cause of thrombosis in pregnancy. We report on two patients with HELLP syndrome who were found to be heterozygous for factor V R506Q mutation, leading to activated protein C resistance. These findings suggest that the pathogenesis of HELLP syndrome is associated with a thrombotic process, and point to the potential benefit of anti-thrombotic therapy in this condition.

journal_name

Br J Haematol

authors

Brenner B,Lanir N,Thaler I

doi

10.1046/j.1365-2141.1996.410947.x

subject

Has Abstract

pub_date

1996-03-01 00:00:00

pages

999-1001

issue

4

eissn

0007-1048

issn

1365-2141

journal_volume

92

pub_type

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