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Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities

2007; Oxford University Press; Volume: 9; Issue: 6 Linguagem: Inglês

10.1093/europace/eum053

1532-2092

Gianfranco Frigo, Alessandra Rampazzo, Barbara Bauce, Kalliopi Pilichou, Giorgia Beffagna, Gian Antonio Danieli, Andrea Nava, Bortolo Martini,

Cardiomyopathy and Myosin Studies

AimsTo describe a patient showing monomorphic ventricular tachycardia, ECG aspect of Brugada syndrome, and structural heart abnormalities due to a homozygous missense mutation in SCN5A.