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

Obstetrics and Gynecology

Volumn 91, Issue 5 II SUPPL., 1998, Pages 812-814

  Kahn, Susan R ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5; HEPARIN; PROTEIN S;

ADULT; ARTICLE; CASE REPORT; DEEP VEIN THROMBOSIS; FEMALE; GENE MUTATION; HEPARINIZATION; HUMAN; PREECLAMPSIA; PRIORITY JOURNAL; PROTEIN S DEFICIENCY; THROMBOPHILIA;

EID: 0031925562     PISSN: 00297844     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0029-7844(97)00713-8     Document Type: Article

References (9)

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2. Hellgren M, Svensson PJ, Dahlbäck B. Resistance to activated protein C as a basis for venous thromboembolism associated with pregnancy and oral contraceptives. Am J Obstet Gynecol 1995;173: 210-3.
3. Dekker GA, de Vries JIP, Doelitzsch PM, Huijgens PC, von Blomberg BME, Jakobs C, et al. Underlying disorders associated with severe early-onset preeclampsia. Am J Obstet Gynecol 1995; 173:1042-8.
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8. Chelsey LC, Cooper DW. Genetics of hypertension in pregnancy: Possible single-gene control of pre-eclampsia and eclampsia in the descendants of eclamptic women. Br J Obstet Gynaecol 1986;93:898-908.
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