Study of common chromosomal abnormalities and Plasminogen activator Inhibitor(PAI-1) gene Polymorphism (5G/4G) and Prothrombin (F2)gene mutation(G20210A) in women with recurrent abortions in the North West of Iran

Study of common chromosomal abnormalities and Plasminogen activator Inhibitor(PAI-1) gene Polymorphism (5G/4G) and Prothrombin (F2)gene mutation(G20210A) in women with recurrent abortions in the North West of Iran

Background. Parental chromosomal abnormalities as well as changes in genes encoding thrombophilic factors are common causes of recurrent abortions. One of the causes of thrombophilia is Factor II (F2) gene mutation (G20210A) and plasminogen activator inhibitor gene (PAI-1) polymorphism (4G/5G). Ther...

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Bibliographic Details
Main Authors: Roya Bagheri, Seyed ali Rahmani, Leila Khoramifar, Solmaz Ilkhichoui
Format: Article
Language:fas
Published: Tabriz University of Medical Sciences 2021-12-01
Series:مجله پزشکی دانشگاه علوم پزشکی تبریز
Subjects:
recurrent miscarriage
plasminogen activator inhibitor-1
chromosomal abnormalities
factor 2 gene
Online Access:https://mj.tbzmed.ac.ir/PDF/mj-43-400.pdf

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