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Reddy, R., Mutreja, D., Mukhopadhyay, I., & Moorchung, N. (2019). Prothrombin gene mutations do not cause recurrent pregnancy loss in the Indian population. International Journal of Reproductive BioMedicine (IJRM), 17(5), 375–376. https://doi.org/10.18502/ijrm.v17i5.4605
https://doi.org/10.18502/ijrm.v17i5.4605
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authors
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Ravindranath Reddy
Ravindranath Reddy
Department of Pathology, Command Hospital Air Force, AGRAM Post, Cambridge Layout, Bangalore, India.
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Deepti Mutreja
Deepti Mutreja
Department of Pathology, Command Hospital Air Force, AGRAM Post, Cambridge Layout, Bangalore, India.
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Indrani Mukhopadhyay
Indrani Mukhopadhyay
Department of Gynaecology and Obstetrics, Command Hospital Air Force, AGRAM Post, Cambridge Layout, Bangalore, India.
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Nikhil Moorchung
Nikhil Moorchung
Department of Pathology, Command Hospital Air Force, AGRAM Post, Cambridge Layout, Bangalore, India.
Published Date
- Jun 18, 2019
Prothrombin gene mutations do not cause recurrent pregnancy loss in the Indian population
Abstract
This is a Letter to the Editor and does not have an abstract.
References
[1] Practice Committee of the American Society for Reproductive Medicine. Definitions of infertility and recurrent pregnancy loss. Fertil Steril 2008; 90 (Suppl.): S60.
[2] Pritchard AM, Hendrix PW, Paidas MJ. Hereditary thrombophilia and recurrent pregnancy loss. Clin Obstet Gynecol 2016; 59: 487–497.
[3] Settin A, Alkasem R, Ali E, ElBaz R, Mashaley AM. Factor V Leiden and prothrombin gene mutations in Egyptian cases with unexplained recurrent pregnancy loss. Hematology 2011; 16: 59–63.
[4] Moussaoui S, Saussoy P, Ambroise J, Defour JP, Zouitene R, Sifi K, et al. Genetic risk factors of venous thromboembolism in the east algerian population. Clin Appl Thromb Hemost 2017; 23: 105–115.
[5] Chudej J, Plameňová I. Prothrombin gene 20210A mutation in Slovak population. Vnitr Lek 2016; 62: 281–286.
[6] Poursadegh Zonouzi A, Chaparzadeh N, Ghorbian S, Sadaghiani MM, Farzadi L, Ghasemzadeh A, et al. The association between thrombophilic gene mutations and recurrent pregnancy loss. J Assist Reprod Genet 2013; 30: 1353–1359.
[7] Mierla D, Szmal C, Neagos D, Cretu R, Stoian V, Jardan D. Association of prothrombin (A20210G) and factor V leiden (A506G) with recurrent pregnancy loss. Maedica (Buchar) 2012; 7: 222–226.
[8] Isaoglu U, Ulug P, Delibas IB, Yilmaz M, Kumtepe Y, Dogan H, et al. The association between inherited thrombophilia and recurrent pregnancy loss in Turkish women. Clin Exp Obstet Gynecol 2014; 41: 177–181.
[9] Munshi A, Aliya N, Jyothy A, Kaul S, Alladi S, Shafi G. Prothrombin gene G20210A mutation is not a risk factor for ischemic stroke in a South Indian Hyderabadi population. Thromb Res 2009; 124: 245–247.
[10] Ghosh K, Shetty S, Madkaikar M, Pawar A, Nair S, Khare A, et al. Venous thromboembolism in young patients from western India: a study. Clin Appl Thromb Hemost 2001; 7: 158–165.
[2] Pritchard AM, Hendrix PW, Paidas MJ. Hereditary thrombophilia and recurrent pregnancy loss. Clin Obstet Gynecol 2016; 59: 487–497.
[3] Settin A, Alkasem R, Ali E, ElBaz R, Mashaley AM. Factor V Leiden and prothrombin gene mutations in Egyptian cases with unexplained recurrent pregnancy loss. Hematology 2011; 16: 59–63.
[4] Moussaoui S, Saussoy P, Ambroise J, Defour JP, Zouitene R, Sifi K, et al. Genetic risk factors of venous thromboembolism in the east algerian population. Clin Appl Thromb Hemost 2017; 23: 105–115.
[5] Chudej J, Plameňová I. Prothrombin gene 20210A mutation in Slovak population. Vnitr Lek 2016; 62: 281–286.
[6] Poursadegh Zonouzi A, Chaparzadeh N, Ghorbian S, Sadaghiani MM, Farzadi L, Ghasemzadeh A, et al. The association between thrombophilic gene mutations and recurrent pregnancy loss. J Assist Reprod Genet 2013; 30: 1353–1359.
[7] Mierla D, Szmal C, Neagos D, Cretu R, Stoian V, Jardan D. Association of prothrombin (A20210G) and factor V leiden (A506G) with recurrent pregnancy loss. Maedica (Buchar) 2012; 7: 222–226.
[8] Isaoglu U, Ulug P, Delibas IB, Yilmaz M, Kumtepe Y, Dogan H, et al. The association between inherited thrombophilia and recurrent pregnancy loss in Turkish women. Clin Exp Obstet Gynecol 2014; 41: 177–181.
[9] Munshi A, Aliya N, Jyothy A, Kaul S, Alladi S, Shafi G. Prothrombin gene G20210A mutation is not a risk factor for ischemic stroke in a South Indian Hyderabadi population. Thromb Res 2009; 124: 245–247.
[10] Ghosh K, Shetty S, Madkaikar M, Pawar A, Nair S, Khare A, et al. Venous thromboembolism in young patients from western India: a study. Clin Appl Thromb Hemost 2001; 7: 158–165.