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

Authors :: Moessmer G
Müller B
Kolben M
Schmitt M
Schneider KT
Artmann A
Source :: Thrombosis and haemostasis [Thromb Haemost] 2005 Apr; Vol. 93 (4), pp. 787-8.
Publication Year :: 2005

Subjects :: Adult
Female
Fetal Growth Retardation genetics
HELLP Syndrome complications
HELLP Syndrome genetics
Homozygote
Humans
Pre-Eclampsia complications
Pregnancy
Thrombophilia complications
Fetal Growth Retardation etiology
HELLP Syndrome etiology
Polymorphism, Single Nucleotide
Prothrombin genetics

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