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 2024/04/23
AB Inherited  mitochondrial  disease  (inborn  error  of  metabolism)  affecting  the  isoleucine  catabolism  resulting  in  recurrent  episodes  of  ketoacidosis.