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 2024/04/24
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.