Genetic Thrombophilia Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A20210 mutations
نویسندگان
چکیده
ELVIRA GRANDONE,* MAURIZIO MARGAGLIONE,* DONATELLA COLAIZZO,* GIUSEPPE PAVONE,° DARIO PALADINI,° PASQUALE MARTINELLI,° GIOVANNI DI MINNO* *Unità di Aterosclerosi e Trombosi and Obstetrics and Gynecology Department, IRCCS “Casa Sollievo della Sofferenza”, S. Giovanni Rotondo (FG); °Obstetrics and Gynecology Department, Università “Federico II”, Naples, Italy Correspondence: Elvira Grandone, MD, Unità di Aterosclerosi e Trombosi, I.R.C.C.S. “Casa Sollievo della Sofferenza”, 71013 San Giovanni Rotondo, Italy. Phone/Fax: international +39.0882.410794. E-mail: [email protected]
منابع مشابه
Inherited Genetic Markers for Thrombophilia in Northeastern Iran (a Clinical-Based Report)
Background: Thrombophilia is a main predisposition to thrombosis due to a procoagulant state. Several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. These thrombophilic mutations are methylenetetrahydrofolate reductase (MTHFR, C677T, and A1298C), factor V Leiden (G1691A), prothrombin gene mutation (factor II, G20210A), and plasminogen...
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Background & Aims:Thromboembolism is an acute cardiovascular disease that ranges from clinically unimportant to massive embolism. Both acquired and hereditary risk factors contribute to the disease. We aimed to determine the prevalence of two hereditary predisposing factor of the disease, prothrombin G20210A and factor V Leiden (G1691A) polymorphisms, in Kerman population.<br /...
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