TY  - CHAP
M1  - Book, Section
TI  - Arginosuccinic Acid Lyase Deficiency
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Marciniak, Bruno
A1  - Dalens, Bernard J.
PY  - 2006
T2  - Syndromes: Rapid Recognition and Perioperative Implications
AB  - Rare  inherited  enzymatic  disorder  characterized  by  severe  hyperammonemia.  Affected  infants  clinically  present  with  vomiting,  lack  of  appetite  and  failure  to  thrive,  progressive  lethargy,  severe  hypotonia,  and  coma.  This  entity  is  part  of  a  group  of  disorders  called  urea  cycle  disorders  (described  later).  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/24
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=58062810
ER  -