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GENATLAS PHENOTYPE

last update : 21-11-2016

Symbol	BRGS5
Location	19q13.12
Name	Brugada syndrome 5
Corresponding gene	SCN1B
Other symbol(s)	BRGDA5
Main clinical features	syncope, sudden cardiac death, or epilepsy, palpitations and dizziness and complete left bundle branch block on electrocardiogram (ECG) characterized by a distinct ST-segment elevation in the right precordial leads of the electrocardiogram and, clinically, by an increased risk of cardiac arrhythmia and sudden death
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Remark(s)