Isolated Non-Compaction of the Ventricular Myocardium Associated With Long QT Syndrome : A Report of 2 Cases
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概要
- 論文の詳細を見る
Isolated non-compaction of the ventricular myocardium (INCVM) is a relatively newly defined clinicopathologic entity. INCVM is clinically accompanied by depressed ventricular function, arrhythmias, and systemic embolization. We report two cases of INCVM with long QT syndrome (LQTS). In both cases the QT interval was over 0.55 s with episodes of torsades de pointes, and prominent ventricular trabeculations and deep intertrabecular recesses were detected by 2-dimensional echocardiography. Both cases had the KCNH2 mutation. To the best of our knowledge, this is the first report investigating INCVM with LQTS. (Circ J 2009; 73: 2169-2172)
- 社団法人 日本循環器学会の論文
- 2009-10-20
著者
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Hoshino Kenji
Division Of Cardiology Saitama Children's Medical Center
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Ando Tatsuya
Division Of Cardiology Saitama Children's Medical Center
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OGAWA Kiyoshi
Division of Cardiology, Saitama Children's Medical Center
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NAKAMURA Yoshihiro
Division of Cardiology, Saitama Children's Medical Center
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TERANO Kazuhiro
Division of Cardiology, Saitama Children's Medical Center
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HISHITANI Takashi
Division of Cardiology, Saitama Children's Medical Center
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Hishitani Takashi
Division Of Cardiology Saitama Children's Medical Center
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Terano Kazuhiro
Division Of Cardiology Saitama Children's Medical Center
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Ogawa Kiyoshi
Division Of Cardiology Saitama Children's Medical Center
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Nakamura Yoshihiro
Division Of Cardiology Saitama Children's Medical Center
関連論文
- Isolated Non-Compaction of the Ventricular Myocardium Associated With Long QT Syndrome : A Report of 2 Cases
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