TY - CHAP M1 - Book, Section TI - Ornithine Carbamoyltransferase Deficiency (OTCD) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164080679 ER -