TY - CHAP M1 - Book, Section TI - Gitelman Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164070829 ER -