TY  - CHAP
M1  - Book, Section
TI  - Multiple Carboxylase Deficiency
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Inborn  error  of  metabolism  present  in  the  neonatal  period  and  characterized  by  tachypnea  or  Kussmaul  breathing,  hypotonia,  and  seizures.  Severe  metabolic  acidosis  with  ketosis  and  hyperammonemia.  If  present  during  infancy  and  childhood,  lethargy,  hypotonia,  seizures  ataxia;  apnea/hyperventilation,  and  frequent  stridor  are  characteristic.  Usually  corrected  with  oral  biotin.  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/10/05
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58076866
ER  -