RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164070829 T1 Gitelman Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164070829 RD 2024/10/15 AB Inherited renal tubular defect resulting in urinary loss of magnesium, sodium, potassium, and chloride with otherwise normal kidneys. Hypokalemic metabolic alkalosis along with hypomagnesemia and hypocalciuria represent the most important features. A prolonged QT interval with possible “torsade de pointes” must be considered as part of serious anesthesia considerations.