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Article

Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia.

American journal of obstetrics and gynecology - 1 Jul 2001

Livingston J C, Barton J R, Park V, Haddad B, Phillips O, Sibai B M

Abstract excerpt

OBJECTIVE: Thrombotic vascular disease may predispose patients to the development of preeclampsia. The purpose of this study was to determine whether maternal or fetal genotype frequencies of the inherited thrombophilic gene mutations (factor V Leiden, methylenetetrahydrofolate, and prothrombin) are altered in severe preeclampsia. STUDY DESIGN: We performed a prospective cross-sectional study to compare the...

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Source

Identifiers

PMID: 11483920
DOI: 10.1067/mob.2001.114691

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia.PMID 11483920Read ↗

Fetal genotype for specific inherited thrombophilias is not associated with severe preeclampsia.Semantic proximity Read ↗

Severe preeclampsia and high frequency of genetic thrombophilic mutations.Semantic proximity Read ↗

Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review.Semantic proximity Read ↗

Maternal factor V Leiden mutation is associated with HELLP syndrome in Caucasian women.Semantic proximity Read ↗

The search for thrombophilic gene mutations in women with gestational hypertension does not help in predicting poor pregnancy outcome.Semantic proximity Read ↗

Inherited thrombophilias are not increased in "idiopathic" small-for-gestational-age pregnancies.Semantic proximity Read ↗

Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women.Semantic proximity Read ↗

Associations between phenotypes of preeclampsia and thrombophilia.Semantic proximity Read ↗

The G20210A prothrombin-gene mutation and the plasminogen activator inhibitor (PAI-1) 5G/5G genotype are associated with early onset of severe preeclampsia.Semantic proximity Read ↗

Inherited thrombophilias and adverse pregnancy outcomes: a case–control study in an Australian populationSemantic proximity Read ↗

Maternal genotype and severe preeclampsia: a HuGE review.Semantic proximity Read ↗

The relationship between thrombophilic mutations and preeclampsia: a prospective case-control study.Semantic proximity Read ↗

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