LONG-QT SYNDROME: A TREATED AND SAVED CASE FROM SUDDEN DEATH

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TABIBAN SASAN; EBADI SEYED KAZEM; GOLSHANI SAMAD; AMINI SEYED MOHAMMAD

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Paper Information

Journal: Journal of Mazandaran University of Medical Sciences Year:2010 | Volume:20 | Issue:78 Page(s): 77-81

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Title

LONG-QT SYNDROME: A TREATED AND SAVED CASE FROM SUDDEN DEATH

Author(s)

TABIBAN SASAN | EBADI SEYED KAZEM | GOLSHANI SAMAD | AMINI SEYED MOHAMMAD | Issue Writer Certificate

Keywords

LONG-QT SYNDROMEQ3

SUDDEN CARDIAC DEATHQ3

POLYMORPHIC VENTRICULAR TACHYCARDIAQ3

SYNCOPEQ3

Abstract

Congenital 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. In 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.

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APA: Copy

TABIBAN, SASAN, EBADI, SEYED KAZEM, GOLSHANI, SAMAD, & AMINI, SEYED MOHAMMAD. (2010). LONG-QT SYNDROME: A TREATED AND SAVED CASE FROM SUDDEN DEATH. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 20(78), 77-81. SID. https://sid.ir/paper/45892/en

Vancouver: Copy

TABIBAN SASAN, EBADI SEYED KAZEM, GOLSHANI SAMAD, AMINI SEYED MOHAMMAD. LONG-QT SYNDROME: A TREATED AND SAVED CASE FROM SUDDEN DEATH. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2010;20(78):77-81. Available from: https://sid.ir/paper/45892/en

IEEE: Copy

SASAN TABIBAN, SEYED KAZEM EBADI, SAMAD GOLSHANI, and SEYED MOHAMMAD AMINI, “LONG-QT SYNDROME: A TREATED AND SAVED CASE FROM SUDDEN DEATH,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 20, no. 78, pp. 77–81, 2010, [Online]. Available: https://sid.ir/paper/45892/en

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