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References OMIM Gene GeneReviews HGMD HGNC
last update : 01-08-2009
Symbol LQT10
Location 11q13
Name long QT syndrome with ventricular tachyarrhythmia, type 10
Corresponding gene KCNE3
Main clinical features
  • characterized by syncopes, seizures predisposing to torsades de pointes, ventricular fibrillation and sudden death, potentially decreasing the outwark K+ currents, leading to a high level of membrane depolarization, including intrauterine and neonatal bradycardia and atrioventricular block
  • Genetic determination autosomal dominant
    Function/system disorder cardiovascular
    Type disease