Frequency of Thrombophilic Gene Mutations in Patients with Deep Vein Thrombosis and in Women with Recurrent Pregnancy Loss

Frequency of Thrombophilic Gene Mutations in Patients with Deep Vein Thrombosis and in Women with Recurrent Pregnancy Loss

Thrombophilia may be anticipated by single or combined hereditary defects in encoding genes factor V, Prothrombin, and MTHFR. The aim of this study was to determine the prevalence and associated risks of V Leiden (G1691A), Prothrombin (G20210A), and MTHFR (C677T) mutations in Saudi women with Deep...

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Bibliographic Details
Main Authors: Elgari Mahmoud Mohamed, Ibrahim Nadir Ahmed, Muddathir Abdel Rahim Mahmoud, Eltoom Faris Mergheni, Ibrahim Ibrahim M
Format: Article
Language:English
Published: De Gruyter 2017-05-01
Series:Open Life Sciences
Subjects:
dvt
factor v (g1691a)
prothrombin (g20210a)
mthfr (c677t)
rpl
pca-nr
Online Access:https://doi.org/10.1515/biol-2017-0019

Internet

https://doi.org/10.1515/biol-2017-0019

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