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Clinical Effects of Serine Medication in Non-ketotic Hyperglycinaemia Due to Deficiency of P-Protein of the Glycine Cleavage Complex

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Studies in Inherited Metabolic Disease

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Abstract

Non-ketotic hyperglycinaemia (McKusick 23830) is an inborn error of metabolism in which, due to a defect in the glycine cleavage reaction, there is accumulation of glycine in plasma and CSF.

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References

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Authors and Affiliations

  1. Department of Pediatrics, University Hospital of Amsterdam (AMC), 1105 AZ, Amsterdam, The Netherlands

    F. A. Wijburg, C. J. de Groot, R. B. H. Schutgens & P. G. Barth

  2. Department of Pediatrics, Tohoku University School of Medicine, Sendai, 980, Japan

    K. Tada

Authors
  1. F. A. Wijburg
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  2. C. J. de Groot
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  3. R. B. H. Schutgens
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  4. P. G. Barth
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  5. K. Tada
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Editor information

R. J. Pollitt R. A. Harkness G. M. Addison

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© 1988 Springer Science+Business Media Dordrecht

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Wijburg, F.A., de Groot, C.J., Schutgens, R.B.H., Barth, P.G., Tada, K. (1988). Clinical Effects of Serine Medication in Non-ketotic Hyperglycinaemia Due to Deficiency of P-Protein of the Glycine Cleavage Complex. In: Pollitt, R.J., Harkness, R.A., Addison, G.M. (eds) Studies in Inherited Metabolic Disease. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-1259-5_36

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  • DOI: https://doi.org/10.1007/978-94-009-1259-5_36

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-7059-1

  • Online ISBN: 978-94-009-1259-5

  • eBook Packages: Springer Book Archive

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