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GENATLAS PHENOTYPE

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

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