Recurrent Pregnancy Loss in a Subject with Heterozygote Factor V Leiden Mutation; a Case Report

Authors

  • Arvin Ghazarian Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  • Mehrdad Sadri Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Mogge Hajesmaeili Department of Biology, Islamic Azad University of Parand, Tehran, Iran.
  • Mohammad Ali Mohammadi Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Mohammad Reza Ezzati Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Najmeh Ranji Department of Genetics, Faculty of Sciences, Islamic Azad University, Rasht Branch, Rasht, Iran.
  • Reza Ebrahimzadeh-Vesal Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  • Roza Azam Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  • Siamak Khavandi Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:

Recurrent pregnancy loss is usually defined as the loss of two or more consecutive pregnancies before 20 weeks of gestation, which occurs in approximately 5% of reproductive-aged women. It has been suggested that women with thrombophilia have an increased risk of pregnancy loss and other adverse pregnancy outcomes. Thrombophilia is an important predisposition to blood clot formation and is considered as a significant risk factor for recurrent pregnancy loss. The inherited predisposition to thrombophilia is most often associated with factor V Leiden mutation, prothrombin G20210A mutation, and methylenetetrahydrofolate reductase C677T and A1298C gene variants. The net effect is an increased cleavage of prothrombin to thrombin and excessive blood coagulation.

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Journal title

volume 2  issue 2

pages  98- 102

publication date 2014-05

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