| hydroxykynureninuria | medical dictionary |
An abnormality in tryptophan metabolism, probably due to a defect in kynureninase, characterised by mild mental retardation, migraine-like headaches, and urinary excretion of large amounts of kynurenine, kynurenine-3-monooxygenase, and xanthurenic acid; autosomal recessive inheritance.
(05 Mar 2000)
hydroxyindoleacetic acid, hydroxyindole oxidase, hydroxyisovalerate dehydrogenase < Prev | Next > hydroxyl, hydroxylamine, hydroxylamine dismutase
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