TY - CHAP M1 - Book, Section TI - Glutaric Acidemia Type II (GA-II) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A 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, heart failure, hypoglycemia, acidosis, muscular hypotonia, characteristic sweaty odorous feet, and death often in the neonatal period. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/03 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164070959 ER -