Home|Journals|Articles by Year|Audio Abstracts
 

Case Report

SETB. 2009; 43(3): 131-133


Cerebral venous thrombosis in a patient with heterozygous methylenetetrahydrofolate reductase (C677T) polymorphism

Sinan Mahir Kayıran, Bülent Zülfikar.




Abstract

Venous thromboembolism is decribed as a multifactorial disorder including both congenital and acquired risk factors and generally detected in elder patients. Although cerebral venous thrombosis (CVT) is associated with substantial mortality and morbidity, its causes in children have not been intensively investigated, mainly because it occurs at a low frequency (0.67 per 100000 children). But the reports of thrombotic events in children are increasing. Methylenetetrahydrofolatereductase (MTHFR) C677 T polymorphism has been detected as an important role in inherited thrombophilia in recent years. In this article we report a child with cerebral venous thrombosis and heterozygous methylenetetrahydrofolatereductase (MTHFR) C677 T polymorphism after otomastoiditis.

Key words: Cerebral venous thrombosis MTHFR (C677T) Polymorphism Otomastoiditis Child Patient






Full-text options


Share this Article


Online Article Submission
• ejmanager.com




ejPort - eJManager.com
Refer & Earn
JournalList
About BiblioMed
License Information
Terms & Conditions
Privacy Policy
Contact Us

The articles in Bibliomed are open access articles licensed under Creative Commons Attribution 4.0 International License (CC BY), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.