Role of Pro564Leu of FXIII-A Gene Polymorphism and Risk of Central Nervous Bleeding in Patients with Congenital Factor XIII Deficiency, Southeast of Iran

Role of Pro564Leu of FXIII-A Gene Polymorphism and Risk of Central Nervous Bleeding in Patients with Congenital Factor XIII Deficiency, Southeast of Iran

Background: The deficiency of factor XIII is a rare hemorrhagic disorder with the highest global incidence in Sistan and Baluchistan province in Iran. Bleeding of central nervous system (CNS) is a common but life-threatening clinical presentation of severe factor XIII deficiency. The aim of this stu...

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Bibliographic Details
Main Authors: Majid Naderi, Akbar Dorgalaleh, Shaban Alizadeh, Ahmad Kazemi, Shadi Tabibian, Hossein Dargahi, Zahra Kashani Khatib, Meysam Kahiri, Maryamsadat Hoseini
Format: Article
Language:fas
Published: Vesnu Publications 2014-04-01
Series:مجله دانشکده پزشکی اصفهان
Subjects:
Factor XIII deficiency
Central nervous system (CNS)
bleeding
Pro564Leu polymorphism
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/3299

Internet

http://jims.mui.ac.ir/index.php/jims/article/view/3299

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