RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164080679
T1 Ornithine Carbamoyltransferase Deficiency (OTCD)
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164080679
RD 2024/04/23
AB Rare  genetic  anomaly  of  the  urea  cycle  characterized  by  complete  or  partial  lack  of  the  enzyme  ornithine  transcarbamylase  (OTC)  resulting  in  hyperammonemia.  Clinically,  patients  present  vomiting,  refusal  to  eat,  progressive  lethargy,  and  coma.