Sudden cardiac arrest during induction of anaesthesia in paediatric patient with glutaric aciduria type II
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Discover STM Publishing Ltd.
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https://www.ejmanager.com/fulltextpdf.php?mno=85393
Reference10 articles.
1. Yamada K, Taketani T. Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency. J Hum Genet. 2019;64:73-85. https://doi.org/10.1038/s10038-018-0527-7
2. Olsen RKJ, Koňaříková E, Giancaspero TA, Mosegaard S, Boczonadi V, Mataković L, et al. Riboflavin-responsive and -Non-responsive mutations in FAD synthase cause multiple Acyl-CoA dehydrogenase and combined respiratory-chain deficiency. Am J Hum Genet. 2016;98:1130-45. https://doi.org/10.1016/j.ajhg.2016.04.006
3. Pooja M, Subasree R, Sumanth S. Multiple Acyl CoA dehydrogenase deficiency: uncommon yet treatable disorder. Neurol India. 2017;65:177-178.
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5. Al-Essa MA, Rashed MS, Bakheet SM, Patay ZJ, Ozand PT. Glutaric aciduria type II: observations in seven patients with neonatal- and late-onset disease. J Perinatol. 2000;20:120-8. https://doi.org/10.1038/sj.jp.7200325
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