RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164061699 T1 Anderson-Tawil Syndrome (ATS) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164061699 RD 2024/11/08 AB An inherited disorder characterized by the clinical triad of potassium-sensitive periodic flaccid paralysis (low, normal, or high potassium levels), ventricular arrhythmias (bigeminy, long-QT interval, ectopy, bidirectional ventricular tachycardia), and dysmorphic facial features. Sudden death has been reported. ATS must not be confused with Andersen Disease (☞Glycogen Storage Disease Type IV).