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hydroxykynureninuria

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hy·drox·y·ky·nu·re·ni·nu·ri·a (h-drks-k-nr-n-nr-)
n.
An inherited abnormality in tryptophan metabolism believed to be due to a defect in kynureninase and characterized by mild mental retardation, migrainelike headaches, and urinary excretion of excessive amounts of kynurenine and xanthurenic acid.


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