Glutathione deficiency as a complication of methylmalonic acidemia: response to high doses of ascorbate.

Treacy, E; Arbour, L; Chessex, P; Graham, G; Kasprzak, L; Casey, K; Bell, L; Mamer, O et al. · J Pediatr · 1996

case_report · Level V

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Abstract

A 7-year-old boy with deficient activity of methylmalonyl coenzyme A mutase (mut-methylmalonic acidemia) was seen in severe metabolic crisis. After hemodialysis and clearance of toxic metabolites, severe lactic acidosis persisted with multiorgan failure. Glutathione deficiency was noted and high-dose ascorbate therapy (120 mg/kg) commenced. Glutathione deficiency may contribute to the lactic acidosis observed during decompensation in patients with methylmalonic acidemia.

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