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- Title
Advancing personalized medicine: the power of collaborative registries of patients with inherited cardiac arrhythmia syndromes.
- Authors
Barsheshet, Alon; Goldenberg, Ilan
- Abstract
These genotype-positive phenotype-negative patients had a significantly lower risk of ACA or SCD compared with LQTS patients with prolonged QTc (4% vs. 15%, respectively, from birth to age 40 years, I P i < 0.001).[10] It is conceivable that in the future, similar low risk groups of I CALM i mutation carriers will also be found. Inherited arrhythmia syndromes without structural heart disease include long QT syndrome (LQTS), Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia (CPVT), short QT syndrome (SQTS), idiopathic ventricular fibrillation (IVF), and other syndromes.
- Subjects
ARRHYTHMIA; CARDIAC patients; INDIVIDUALIZED medicine; BRUGADA syndrome; MEDICAL registries; CONGENITAL heart disease
- Publication
European Heart Journal, 2023, Vol 44, Issue 35, p3371
- ISSN
0195-668X
- Publication type
Article
- DOI
10.1093/eurheartj/ehad441