Idiopathic short QT interval: A new clinical syndrome?
Idiopathic short QT interval: A new clinical syndrome?
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DOI：
10.1159/000047299
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发表时间：
2000-01-01
期刊：
影响因子：
1.9
通讯作者：
Bjerregaard, P
中科院分区：
文献类型：
--
作者：
Gussak, I;Brugada, P;Bjerregaard, P
在这个特发性家族性持续短QT间期（QTI）的第一份临床报告中，我们描述了一个家庭的三名成员（一名17岁的女性，她21岁的哥哥和他们51岁的母亲）表现出这种ECG现象，17岁的患者伴有几次阵发性心房颤动，需要电转复。在一名无关的37岁患者中也发现了类似的心电图变化与心源性猝死有关。我们的报告还描述了QTI异常缩短的其他表现，并考虑了短QTI可能的致心律失常的潜力，版权(C) 2001 S. Karger AG。巴塞尔协议。
In this first clinical report of an idiopathic familial persistently short QT interval (QTI), we describe three members of one family (a 17-year-old female, her 21-year-old brother, and their 51-year-old mother) demonstrating this ECG phenomenon, associated in the 17-year-old with several episodes of paroxysmal atrial fibrillation requiring electrical cardioversion. Similar ECG changes seen in an unrelated 37-year-old patient were associated with sudden cardiac death. Our report also describes other manifestations of abnormal shortening of the QTI and considers the possible arrhythmogenic potential of the short QTI, Copyright (C) 2001 S. Karger AG. Basel.