TY - CHAP M1 - Book, Section TI - Familial Hyperlysinemia A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - The enzyme deficiencies of α-aminoadipic semialdehyde dehydrogenase and the saccharopine dehydrogenases have been associated with increased serum levels of L-lysine. The clinical presentation is very variable and may include developmental delay, hypotonia, lethargy recurrent emesis, and diarrhea. The use of anesthetics deemed to be safe in malignant hyperthermia (MH)-susceptible patients produced an uneventful perioperative course. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164069515 ER -