The long QT syndrome
Copyright policy )The long QT syndrome
The Long QT syndrome (LQTS) is an inherited arrhythmogenic disease occurring in the structurally normal heart that may cause sudden death and that usually manifests in children and teen-agers (1). The prevalence of this disorder is still undefined, however it is estimated to be between 1:10000–1:5000.
- University of Milano-Bicocca Italy
- IRCCS Italy
- University of Pavia Italy
- Istituti di Ricovero e Cura a Carattere Scientifico Italy
- Fondazione Salvatore Maugeri Italy
ERG1 Potassium Channel, Potassium Channels, Sympathetic Nervous System, Adrenergic beta-Antagonists, Cardiac Pacing, Artificial, Electric Countershock, Ether-A-Go-Go Potassium Channels, DNA-Binding Proteins, Diagnosis, Differential, Electrocardiography, Long QT Syndrome, Transcriptional Regulator ERG, LONG QT SYNDROME, Heart Rate, Potassium Channels, Voltage-Gated, Trans-Activators, Humans, Genetic Predisposition to Disease, Sympathectomy, Cation Transport Proteins, Molecular Biology
ERG1 Potassium Channel, Potassium Channels, Sympathetic Nervous System, Adrenergic beta-Antagonists, Cardiac Pacing, Artificial, Electric Countershock, Ether-A-Go-Go Potassium Channels, DNA-Binding Proteins, Diagnosis, Differential, Electrocardiography, Long QT Syndrome, Transcriptional Regulator ERG, LONG QT SYNDROME, Heart Rate, Potassium Channels, Voltage-Gated, Trans-Activators, Humans, Genetic Predisposition to Disease, Sympathectomy, Cation Transport Proteins, Molecular Biology
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