Successful perioperative management of living-donor liver transplantation for a patient with severe methylmalonic acidemia: a case report
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Baumgartner MR, Hörster F, Dionisi-Vici C, et al. Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia. Orphanet J Rare Dis. 2014. https://doi.org/10.1186/s13023-014-0130-8.
Zwickler T, Haege G, Riderer A, et al. Metabolic decompensation in methylmalonic aciduria: which biochemical parameters are discriminative? J Inherit Metab Dis. 2012;35:797–806.
Spada M, Calvo PL, Brunati A, et al. Early liver transplantation for neonatal-onset methylmalonic acidemia. Pediatrics. 2015;136:e252–6.
Baba C, Kasahara M, Kogure Y, et al. Perioperative management of living-donor liver transplantation for methylmalonic acidemia. Pediatr Anesth. 2016;26:694–702.
Chalmers RA, Roe CR, Stacey TE, Hoppel CE. Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine. Pediatr Res. 1984;18:1325–8.
Sanders RD, Weimann J, Maze M. Biologic effects of nitrous oxide: a mechanistic and toxicologic review. Anesthesiology. 2008;109:707–22.
Court MH, Duan SX, Hesse LM, et al. Cytochrome P-450 2B6 is responsible for interindividual variability of propofol hydroxylation by human liver microsomes. Anesthesiology. 2001;94:110–9.
Ktena YP, Ramstad T, Baker EH, et al. Propofol administration in patients with methylmalonic acidemia and intracellular cobalamin metabolism disorders: a review of theoretical concerns and clinical experiences in 28 patients. J Inherit Metab Dis. 2015;38:847–53.
Julie N, Phil GM. Anesthetic considerations in patients with mitochondrial defects. Paediatr Anaesth. 2013;23:785–93.