References
Daras BT, Friedman NR (2000) Metabolic myopathy: a clinical approach. Pediatr Neurol 22:87–97
Chi CS, Mak SC, Shian WJ, Chen CH (1992) Oral glucose lactate stimulation test in mitochondrial disease. Pediatr Neurol 8:445–449
Chromyn A, Martinuzzi A, Yoneda M, Daga A, Hurko O, Johns D, Lai ST, Nonaka I, Angelini C, Attardi G (1992) MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcript. Proc Natl Acad Sci USA 89:4221–4225
Levinger L, Oestreich I, Florentz C, Mörl M (2004) A pathogenesis-associated mutation in human mitochondrial tRNALeu (UUR) leads to reduced 3’-end processing and CCA addition. J Mol Biol 337:535–544
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This refers to the article that can be found at http://dx.doi.org/10.1007/s00467-015-3152-0.
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Tseng, MH., Hsia, SH., Chi, CS. et al. Exertional rhabdomyolysis, profound lactic acidosis, and acute kidney injury in a young boy: Answers. Pediatr Nephrol 31, 1607–1610 (2016). https://doi.org/10.1007/s00467-015-3150-2
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DOI: https://doi.org/10.1007/s00467-015-3150-2