RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58076320 T1 Mitochondrial Acetoacetyl-CoA Thiolase (ACAT) 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=58076320 RD 2024/10/15 AB Inherited mitochondrial disease (inborn error of metabolism) affecting the isoleucine catabolism resulting in recurrent episodes of ketoacidosis.