RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Marciniak, Bruno
A1 Dalens, Bernard J.
SR Print(0)
ID 58065615
T1 Carnitine Palmitoyltransferase Deficiency
T2 Syndromes: Rapid Recognition and Perioperative Implications
YR 2006
FD 2006
PB The McGraw-Hill Companies
PP New York, NY
SN 9780071354554
LK accessanesthesiology.mhmedical.com/content.aspx?aid=58065615
RD 2024/04/23
AB Carnitine  palmitoyltransferase  (CPT)  deficiency  is  a  group  of  disorders  caused  by  defects  in  the  enzymes  CPT  I  or  II.  Type  I  is  the  most  common  human  lipid  myopathy.  The  metabolic  myopathy  can  be  triggered  by  effort,  anesthesia/surgery,  or  stress  and  results  in  episodes  of  rhabdomyolysis  and  myoglobinuria.