scholarly journals Short QT interval

2013 ◽  
Vol 11 (1) ◽  
pp. 92-94
Author(s):  
Bijondra Kumar Rai

Introduction: Short QT Interval (Short QT Syndrome) is a very rare clinical condition. An individual with short QT interval frequently presents with chest pain, palpitation, fainting attack and sometimes cardiac death. Objective: To report a case of Short QT Syndrome. Case: A 27 year old man presented with the complaint of frequent attack of chest pain, palpitation and fainting attack for last one and half years. The ECG revealed short QT interval of 300ms without any cardiac abnormalities. Conclusion: The short QT interval (Short QT Syndrome) is one of the causes of palpitation, chest pain, dizziness and syncope in a young person. Early detection is possible by doing ECG. So ECG is advised to all adults complaining of frequent chest pain, unexplained fainting attack. Health Renaissance, January-April 2013; Vol. 11 No.1; 92-94 DOI: http://dx.doi.org/10.3126/hren.v11i1.7611

2020 ◽  
Vol 75 (11) ◽  
pp. 469
Author(s):  
Juan Jiménez Jáimez ◽  
Francisco Bermúdez ◽  
Ana Moreno-Manuel ◽  
Lilian Gutiérrez Espinosa de los Monteros ◽  
María Linarejos Vera-Pedrosa ◽  
...  

2020 ◽  
pp. 88-92
Author(s):  
T.V. Tolstikova ◽  
◽  
L.V. Bregel ◽  
S.V. Czurkan ◽  
T.P. Marchuk ◽  
...  

A clinical family case of Jervell and Lange-Nielsen syndrome in 2 children is presented. Long QT syndrome is one of the leading causes of sudden cardiac death in children. Jervell and Lange-Nielsen syndrome is one of the most severe and rare types of long QT syndrome. Symptoms of the disease appear in infancy; they are characterized by a lengthening of QT interval on ECG, syncope as a result of life-threatening ventricular tachycardia and ventricular fibrillation, combined with congenital bilateral hearing loss.


2017 ◽  
Vol 38 (suppl_1) ◽  
Author(s):  
C. Scrocco ◽  
C. Giustetto ◽  
M. Callegari ◽  
P. Maury ◽  
E. Tulumen ◽  
...  

2009 ◽  
Vol 25 (4) ◽  
pp. 214-218 ◽  
Author(s):  
Kaoru Okishige ◽  
Koji Sugiyama ◽  
Minetaka Maeda ◽  
Hideshi Aoyagi ◽  
Manabu Kurabayashi ◽  
...  

2017 ◽  
Vol 19 (2) ◽  
pp. 15-22
Author(s):  
S N Kolyubaeva

The review presents the recent data on genetic reasons of sudden cardiac death. Mutations discuss in gens associated with sudden cardiac death. Channalopathies, such as Brugada syndrome, long QT syndrome, short QT syndrome and catecholaminergic polymorphic ventricular tachycardia are characterized by arrhythmias in normal heart resulting from genetic anomalies in ion channels


2012 ◽  
Vol 8 (3) ◽  
pp. 41 ◽  
Author(s):  
I. Comelli ◽  
G. Lippi ◽  
G. Mossini ◽  
G. Gonzi ◽  
T. Meschi ◽  
...  

Author(s):  
Maria Lícia Ribeiro Cury Pavão ◽  
Viviane Cristina Ono ◽  
Elerson Arfelli ◽  
Marcus Vinícius Simões ◽  
José Antonio Marin Neto ◽  
...  

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