TY - CHAP M1 - Book, Section TI - Argininosuccinic Acid Lyase Deficiency (ASLD) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - An inherited urea cycle disorders characterized by severe hyperammonemia. Affected infants present with vomiting, lack of appetite and failure to thrive, severe hypotonia, progressive lethargy, and coma. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164061921 ER -