TY - CHAP M1 - Book, Section TI - Anderson-Tawil Syndrome (ATS) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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). SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164061699 ER -