Volume 20, Issue 78 (May 2010)
J Mazandaran Univ Med Sci 2010, 20(78): 77-81 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Tabiban S, Ëbadi K, Golshani S, Âmini S. Long-QT Syndrome: A Treated and Saved Case from Sudden Death. J Mazandaran Univ Med Sci 2010; 20 (78) :77-81
URL: http://jmums.mazums.ac.ir/article-1-628-en.html
URL: http://jmums.mazums.ac.ir/article-1-628-en.html
Abstract: (15489 Views)
Çongenital long-QT syndrome (LQTS) is an inherited disorder that presents with syncope, polymorphic ventricular tachycardia, torsade de pointes and sudden death. The incidence rate of LQTS is 1 to 2 per 100000 and mainly involves children and young individuals. Because of familial and genetic underling and predisposing factors for life threatening arrhythmias in patients, diagnosis and treatment are an important aspects in the management of this syndrome. Ïn this study LQTS is described in a 49 years old woman with syncope, ventricular fibrillation and torsade de pointes who was referred to the Fatemeh Zahra (S) teaching hospital and treated successfully.
Type of Study: Research(Original) |
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
Articles Copyright © The Author(s). Owned by Mazandaran University of Medical Sciences.
Contact Us
Address: Journal Office, Building No. 2, Mazandaran University of Medical Sciences, Moallem Square, Sari.Tel: +98 (011)34484874 Postal code: 48175-866 E-Mail: jmums@mazums.ac.ir Telefax: +98 (011)33262679
