TY  - CHAP
M1  - Book, Section
TI  - Glutaric Acidemia Type II (GA-II)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
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.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58077956
ER  -