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Research Article

Non-ketotic hyperglycinaemia: case report and review of medical literature

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Pages 537-539 | Received 06 Feb 2011, Accepted 23 Oct 2012, Published online: 29 Nov 2012

References

  • Lang TF,Parr JR, Matthews EE, Gray RGF, Bonham JR, Kay JDS. Practical difficulties in the diagnosis of transient non-ketotic hyperglycinaemia, 2007.
  • Kliegman RM, Behrman RE, Jenson HB, Stanton BF. Nelson’s Textbook of Paediatrics. 16th edn., 2000, Philadelphia PA. Saunders, Elsevier.
  • Fletcher JM, Bye AM, Nayanar V, Wilcken B. Non-ketotic hyperglycinaemia presenting as pachygyria. J Inherit Metab Dis 1995;18:665–668.
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  • Hoover-Fong JE, Shah S, Van Hove JL, Applegarth D, Toone J, Hamosh A. Natural history of nonketotic hyperglycinemia in 65 patients. Neurology 2004;63:1847–1853.
  • Pueschel SM, Cha CJ, Langon T. Therapeutic attempts in infants with nonketotic hyperglycinaemia. J Ment Defic Res 1981;25:61–69.
  • Hui HNT, Ho YC, Chan HB, Tam SCF, Tang NLS, Ip PLSI. A baby with non-ketotic hyperglycinaemia. J Paediatr 2004;9:243–247.
  • Kazmierczuk-Skubis ME, Zatorska-Karpus M, Pac-Kozuchowska E, Bojko-Jaworska J, Furmaga-Jablonska W. Non-ketotic hyperglycinemia as the cause of infant seizures–the case study. Ann Univ Mariae Curie Sklodowska Med 2004;59:237–241.
  • Lang TF, Parr JR, Matthews EE, Gray RDF, Bonham JR. Kay JDS: Developmental Medicine & Child Neurology 2008;50:157–159.

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