TY - JOUR
T1 - Syncope in hereditary arrhythmogenic syndromes
AU - Adler, Arnon
AU - Viskin, Sami
PY - 2013/12
Y1 - 2013/12
N2 - Since the discovery of the first mutation causing long QT syndrome (LQTS) in 1995, the field of hereditary arrhythmogenic syndromes has expanded greatly. Today, these syndromes include LQTS, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. There is also evidence suggesting that the newly described malignant early repolarization syndrome also has a genetic cause.
AB - Since the discovery of the first mutation causing long QT syndrome (LQTS) in 1995, the field of hereditary arrhythmogenic syndromes has expanded greatly. Today, these syndromes include LQTS, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. There is also evidence suggesting that the newly described malignant early repolarization syndrome also has a genetic cause.
KW - Arrhythmogenic syndrome
KW - Follow-up
KW - Genotype
KW - Syncope
UR - http://www.scopus.com/inward/record.url?scp=84887533543&partnerID=8YFLogxK
U2 - 10.1016/j.ccep.2013.08.005
DO - 10.1016/j.ccep.2013.08.005
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AN - SCOPUS:84887533543
SN - 1877-9182
VL - 5
SP - 479
EP - 486
JO - Cardiac Electrophysiology Clinics
JF - Cardiac Electrophysiology Clinics
IS - 4
ER -