RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164064597
T1 Carnitine Palmitoyltransferase Deficiency
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=1164064597
RD 2024/04/25
AB Carnitine  Palmitoyltransferase  (CPT)  Deficiency  comprises  a  group  of  disorders  caused  by  decreased  activity  of  the  enzymes  CPT  I  or  II.  Type  II  is  the  most  common  human  lipid  myopathy.  The  metabolic  myopathy  can  be  triggered  by  exercise,  anesthesia/surgery,  or  stress  and  results  in  episodes  of  rhabdomyolysis  and  myoglobinuria.