TY - CHAP M1 - Book, Section TI - Phosphoenolpyruvate Carboxykinase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Congenital metabolic disease leading to defect of gluconeogenesis and severe acidemia. Other clinical features include hypotonia, hypoglycemia, hepatomegaly, and growth delay. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164081679 ER -