Abstract
IN recent years several reports1–3 have called attention to a disorder occurring in the paediatric age group which is characterized by marked over-production of uric acid. The clinical features include haematuria and uric acid stone disease, and often, but not always, mental retardation, neurological signs, and self-mutilation. Intravenous injection of glycine-14C into such patients results in a rapid incorporation1 of isotope into urinary uric acid, signifying the presence of a shunt pathway whereby precursor is incorporated into uric acid without previous incorporation into nucleic acid purines.
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References
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SORENSEN, L., BENKE, P. Biochemical Evidence for a Distinct Type of Primary Gout. Nature 213, 1122–1123 (1967). https://doi.org/10.1038/2131122b0
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DOI: https://doi.org/10.1038/2131122b0
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