Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 21-11-2016

Symbol	BRGS7
Location	11q24.1
Name	Brugada syndrome 7
Corresponding gene	SCN3B
Other symbol(s)	BRGDA7
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
Prevalence	rare cause of Brugada syndrome
Function/system disorder	cardiovascular
Type	disease

Remark(s)