Literature DB >> 9572171

Severe preeclampsia associated with coinheritance of factor V Leiden mutation and protein S deficiency.

S R Kahn1.   

Abstract

BACKGROUND: Inherited thrombophilic disorders are associated with an increased risk of venous thromboembolism during pregnancy. Preliminary research suggests that these disorders might also increase the risk for preeclampsia. CASE: A 29-year-old primigravida developed severe, early onset preeclampsia and postpartum deep venous thrombosis. Subsequent testing revealed coinheritance of the factor V Leiden mutation and protein S deficiency. Heparin prophylaxis was administered during two subsequent pregnancies without recurrence of either preeclampsia or venous thromboembolism.
CONCLUSION: Our patient's inherited thrombophilia may have played a role in the development of preeclampsia, and anticoagulation during subsequent pregnancies may have prevented preeclampsia recurrence. An association between inherited thrombophilic disorders and preeclampsia is biologically plausible.

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Year:  1998        PMID: 9572171     DOI: 10.1016/s0029-7844(97)00713-8

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  2 in total

1.  Alexia without agraphia in a postpartum eclamptic patient with factor V Leiden deficiency.

Authors:  Haideh Yazdani Sabet; Pamela Blake; Dan Nguyen
Journal:  AJNR Am J Neuroradiol       Date:  2004-03       Impact factor: 3.825

2.  Hypertension in pregnancy: new recommendations for management.

Authors:  R Shear; L Leduc; E Rey; J M Moutquin
Journal:  Curr Hypertens Rep       Date:  1999-12       Impact factor: 5.369

  2 in total

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