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Preliminary report on mellituria in phenylketonuric children: Modification in the excretion of glucose and pentoses

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Journal of Inherited Metabolic Disease

Abstract

Urine from children with phenylketonuria contains less glucose and more pentoses than urine from normal children.

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References

  • Lipovac, K., Zanic-Grubisč, T., Mihaljevic, J. and Fuks, Z. Disturbances of energy metabolism in rats with experimentally induced hyperphenylalaninemia. In Hommes, F. A. (ed.)Models for the Study of Inborn Errors of Metabolism, Elsevier-North Holland Biomedical Press, Amsterdam, 1979, pp. 133–140

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  • Piccardo, M. G., Rosa, M., Russo, L. and De Santis, R. La melituria nei pazienti cistinurici.Progr. Medico. 35 (1979) 135

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  • Piccardo, M. G., Rosa, M., Russo, L. and De Santis, R. La melituria nei diabetici.Progr. Medico. 36 (1980) 179

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  • Zanic-Grubisič, T. and Lipovac, K. Disturbances of the amino acid transport in rats with experimental hyperphenylalaninaemia.J. Inher. Metab. Dis. 4 (1981) 105–106

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Authors and Affiliations

  1. IIo Medical Clinic, University of Rome, Rome, Italy

    M. G. Piccardo, M. Rosa & L. Russo

Authors
  1. M. G. Piccardo
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  2. M. Rosa
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  3. L. Russo
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Piccardo, M.G., Rosa, M. & Russo, L. Preliminary report on mellituria in phenylketonuric children: Modification in the excretion of glucose and pentoses. J Inherit Metab Dis 4, 87–88 (1981). https://doi.org/10.1007/BF02263604

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  • DOI: https://doi.org/10.1007/BF02263604

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