TY - CHAP M1 - Book, Section TI - Carnitine Palmitoyltransferase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164064597 ER -