@misc{cogprints4278,
          volume = {3},
          number = {3},
           month = {July},
          author = {Berardo Sarubbi and Pasquale Vergara and Michele D?Alto and Raffaele Calabr{\`o}},
          editor = {Balbir Singh and Yash Lokhandwala and Johnson Francis and Anup Gupta},
           title = {Congenital Junctional Ectopic Tachycardia: Presentation And Outcome},
       publisher = {Indian Pacing and Electrophysiology Group},
            year = {2003},
         journal = {Indian Pacing and Electrophysiology Journal},
           pages = {143--147},
        keywords = {Junctional Ectopic Tachycardia, Congenital },
             url = {http://cogprints.org/4278/},
        abstract = {Junctional ectopic tachycardia (JET) is a rare type of supraventricular arrhythmia. Even if its management has improved in recent years, it remains a great challenge for the cardiologist. Two are the possible clinical presentations of this arrhythmia: as a primary idiopathic disorder during infancy, configuring the so called ?congenital? JET, or more often as a transient phenomenon immediately after surgery for congenital heart disease, giving rise to the ?post-operative? variety. 
            The congenital form, firstly described as a distinct entity by Coumel et al. in 19761, usually occurs in the first six months of life presenting as a persistent sustained form, lasting up to 90\% of the time. Its clinical presentation may be dramatic, being associated in up to 60\% of cases with cardiomegaly and/or heart failure. 
            Congenital JET is hampered by high mortality. Secondary dilated cardiomyopathy, ventricular fibrillation and sudden cardiac death have also been reported 2,3.
}
}

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