Congenital short QT syndrome: Landmarks of the newest arrhythmogenic cardiac channelopathy

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Congenital short QT syndrome: landmarks of the newest arrhythmogenic cardiac channelopathy.

Congenital or familial short QT syndrome is a genetically heterogeneous cardiac channelopathy without structural heart disease that has a dominant autosomal or sporadic pattern of transmission affecting the electric system of the heart. Patients present clinically with a spectrum of signs and symptoms including irregular palpitations due to episodes of paroxysmal atrialfibrillation, dizziness a...

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Congenital Short QT Syndrome

Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital long QT syndrome was first described in individuals with structurally normal hearts in 1957.1 Little was known about the significance of a short QT interval. In 1993, after analyzing 6693 consecutive Holter recordings Algra et al concluded that an increased risk of sudden death was present not only ...

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Congenital Short QT Syndrome

The Short QT Syndrome is a recently described new genetic disorder, characterized by abnormally short QT interval, paroxysmal atrial fibrillation and life threatening ventricular arrhythmias. This autosomal dominant syndrome can afflict infants, children, or young adults; often a remarkable family background of cardiac sudden death is elucidated. At electrophysiological study, short atrial and ...

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Mailing Address: André Schmidt • Avenida dos Bandeirantes n 3900 Bairro Campus Universitario Monte Alegre Postal Code 14048-900 Ribeirão Preto, São Paulo, SP Brazil E-mail: [email protected], [email protected] Manuscript received May 23, 2013; revised manuscript July 03, 2013; accepted December 17, 2013.

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ژورنال

عنوان ژورنال: Cardiology Journal

سال: 2013

ISSN: 1898-018X,1897-5593

DOI: 10.5603/cj.a2013.0052