HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A

Georg Moessmer; Burkhardt Müller; Martin Kolben; Manfred Schmitt; Karl Theodor Maria Schneider; Almut Artmann

doi:10.1055/s-0037-1616784

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2005; 93(04): 787-788
DOI: 10.1055/s-0037-1616784

Case Report

Schattauer GmbH

HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A

Authors

Georg Moessmer

¹Institute for Clinical Chemistry, Technische Universität München, Klinikum rechts der Isar, München, Germany
Burkhardt Müller

¹Institute for Clinical Chemistry, Technische Universität München, Klinikum rechts der Isar, München, Germany
Martin Kolben

²Department of Obstetrics and Gynaecology, Technische Universität München, Klinikum rechts der Isar, München, Germany
Manfred Schmitt

²Department of Obstetrics and Gynaecology, Technische Universität München, Klinikum rechts der Isar, München, Germany
Karl Theodor Maria Schneider

²Department of Obstetrics and Gynaecology, Technische Universität München, Klinikum rechts der Isar, München, Germany
Almut Artmann

²Department of Obstetrics and Gynaecology, Technische Universität München, Klinikum rechts der Isar, München, Germany

Abstract

Full Text

References

References
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