TY - CHAP M1 - Book, Section TI - Histidinemia A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Histidinemia is a rare hereditary metabolic disorder characterized by a deficiency of the enzyme histidase, which is necessary for the metabolism of the amino acid histidine. The majority of individuals are asymptomatic. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/19 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164073019 ER -