Short QT Syndrome in a Pediatric Patient

被引:12
|
作者
Villafane, Juan [2 ]
Young, Ming Lon [3 ]
Maury, Philippe [4 ]
Wolpert, Christian [5 ]
Anttonen, Olli [6 ]
Hamilton, Robert [7 ]
Kannankeril, Prince J. [8 ]
Fischbach, Peter S. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Pediat, Sibley Heart Ctr Cardiol, Atlanta, GA 30307 USA
[2] Childrens Heart Specialists, Louisville, KY USA
[3] Univ Miami, Dept Pediat, Miami, FL 33152 USA
[4] Univ Hosp Rangueil, Toulouse, France
[5] Univ Heidelberg, Heidelberg, Germany
[6] Paijat Hame Cent Hosp, Dept Med, Lahti, Finland
[7] Univ Toronto, Dept Pediat, Toronto, ON, Canada
[8] Vanderbilt Univ, Dept Pediat, Nashville, TN USA
关键词
Channelopathy; Arrhythmia; Sudden death; Syncope; CARDIOVERTER-DEFIBRILLATOR TREATMENT; SUDDEN CARDIAC DEATH; PROGNOSTIC-SIGNIFICANCE; INTERVAL; MUTATION; HERG; GENE;
D O I
10.1007/s00246-009-9439-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Short QT syndrome (SQTS) is a recently described genetic syndrome characterized by abnormally brisk ventricular repolarization. Similar to long QT syndrome, SQTS might result in ventricular arrhythmias, syncope, and sudden death. The clinical diagnosis of SQTS is supported by the finding of an abnormally short QT interval on the resting electrocardiogram in combination with a suggestive clinical or family history. To date, few pediatric cases have been reported and the ideal therapy is unknown. We report a teenage boy who suffered a witnessed ventricular fibrillation arrest and was subsequently diagnosed with SQTS. Additional data from nine other pediatric patients diagnosed with SQTS are presented.
引用
收藏
页码:846 / 850
页数:5
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