Dilated Cardiomyopathy with Short QT Interval: Is It a New Clinical Entity?

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dc.contributorBohora, Shomu
dc.contributorNamboodiri, Narayanan
dc.contributorTharakan, Jaganmohan
dc.contributorVk, Ajit Kumara
dc.contributorNayyar, Sachin
dc.date.accessioned2012-12-04T11:43:52Z
dc.date.available2012-12-04T11:43:52Z
dc.date.issued2009
dc.description.abstractShort QT syndrome is a rare autosomal dominant channelopathy of structurally normal hearts characterized by atrial fibrillation, ventricular arrhythmias, and sudden cardiac death. We report a case having short QT, dilated ventricles, and severe ventricular dysfunction, an unreported association so far. (PACE 2009; 32:688-690)
dc.identifier.citationPACE-PACING AND CLINICAL ELECTROPHYSIOLOGY. 32; 5; 688-690en_US
dc.identifier.urihttp://dx.doi.org/10.1111/j.1540-8159.2009.02349.x
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/19422597
dc.identifier.urihttps://dspace.sctimst.ac.in/handle/123456789/370
dc.publisherPACE-PACING AND CLINICAL ELECTROPHYSIOLOGY
dc.subjectCardiology
dc.titleDilated Cardiomyopathy with Short QT Interval: Is It a New Clinical Entity?
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