Abstract
The congenital long-QT syndrome is characterized by prolonged ventricular repolarization and life-threatening arrhythmias. Two variants of the disease are recognized: the autosomal recessive Jervell and Lange-Nielsen syndrome, characterized by prolonged repolarization and congenital deafness; and the autosomal dominant Romano-Ward syndrome, also marked by prolonged repolarization but with normal hearing. Recent studies have shown …
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