Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1

Volume: 75, Issue: 15, Pages: 1772 - 1784
Published: Apr 1, 2020
Abstract
Andersen-Tawil Syndrome type 1 (ATS1) is a rare arrhythmogenic disorder, caused by loss-of-function mutations in the KCNJ2 gene. We present here the largest cohort of patients with ATS1 with outcome data reported. This study sought to define the risk of life-threatening arrhythmic events (LAE), identify predictors of such events, and define the efficacy of antiarrhythmic therapy in patients with ATS1. Clinical and genetic data from consecutive...
Paper Details
Title
Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1
Published Date
Apr 1, 2020
Volume
75
Issue
15
Pages
1772 - 1784
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