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Case Reports
. 1986;9(2):186-92.
doi: 10.1007/BF01799457.

A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet

Case Reports

A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet

L R Gjessing et al. J Inherit Metab Dis. 1986.

Abstract

The characteristic biochemical disturbances of the amino acid and pyrimidine metabolism are described and illustrated by the first case of the HHH syndrome reported in Norway. The disorder was treated with a low protein diet at an early age and the patient developed normally on this diet.

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References

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    1. J Inherit Metab Dis. 1982;5(1):41-7 - PubMed
    1. Clin Chim Acta. 1982 Feb 5;118(2-3):149-57 - PubMed
    1. Am J Dis Child. 1969 Jan;117(1):83-92 - PubMed
    1. J Inherit Metab Dis. 1984;7(4):147-50 - PubMed

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