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The use of amino acid supplements in inherited metabolic disease

  • SSIEM SYMPOSIUM 2005
  • Published:
Journal of Inherited Metabolic Disease

Summary

Amino acid supplements are recognized to be essential for the management of a number of inherited metabolic disorders but their use in some other conditions is more controversial.

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Abbreviations

MELAS:

mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

NMDA:

N-methyl-D-aspartate

PKU:

phenylketonuria

References

  • de Koning TJ, Duran M, Dorland L, et al (1998) Beneficial effects of l-serine and glycine in the management of seizures in 3-phosphoglycerate dehydrogenase deficiency. Ann Neurol 44(2): 261–265.

    Article  PubMed  Google Scholar 

  • Koch R, Moseley KD, Yano S, et al (2003) Large neutral amino acid therapy and phenylketonuria: a promising approach to treatment. Mol Genet Metab 79(2): 110–113.

    Article  PubMed  CAS  Google Scholar 

  • Koga Y, Akita Y, Nishioka J, et al (2005) l-Arginine improves the symptoms of strokelike episodes in MELAS. Neurology 64(4): 710–712.

    PubMed  CAS  Google Scholar 

  • Kolker S, Garbade SF, Greenberg CR, et al (2006) Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency. Pediatr Res (in press)

  • Matsuo S, Inoue F, Takeuchi Y, et al (1995) Efficacy of tryptophan for the treatment of nonketotic hyperglycinemia: a new therapeutic approach for modulating the N-methyl-d-aspartate receptor. Pediatrics 95(1): 142–146.

    PubMed  CAS  Google Scholar 

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Additional information

Communicating editor: Jean-Marie Saudubray

Competing interests: None declared

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Walter, J.H., MacDonald, A. The use of amino acid supplements in inherited metabolic disease. J Inherit Metab Dis 29, 279–280 (2006). https://doi.org/10.1007/s10545-006-0357-1

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  • DOI: https://doi.org/10.1007/s10545-006-0357-1

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