RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58077956 T1 Glutaric Acidemia Type II (GA-II) 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=58077956 RD 2024/03/29 AB Progressive neurologic disorder caused by a genetically transmitted inborn error of metabolism in which the body cannot oxidize fatty acids. Typical clinical features include respiratory distress, muscular hypotonia, sweaty odorous feet, and death often in the neonatal period.