Familial Hydroxykynureninuria

During a survey of aminoacidopathies in the patients in various hospitals in the city, a Hindu joint family with increased urinary excretion of kynurenine, 3-hydroxykynurenine and xanthurenic acid was detected.

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Bibliographic Details
Published in:Human heredity 1978, Vol.28 (3), p.238-240
Main Authors: Reddi, O. S., Reddy, M. V. R.
Format: Article
Language:English
Subjects:
Amino Acid Metabolism, Inborn Errors - genetics
Amino Acid Metabolism, Inborn Errors - urine
Child
Consanguinity
Female
Gingival Diseases - genetics
Humans
Inborn Errors of Metabolism in Man
Intellectual Disability - genetics
Kynurenine - analogs & derivatives
Kynurenine - urine
Male
Pedigree
Stomatitis - genetics
Syndrome
Tryptophan - metabolism
Xanthurenates - urine
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Description
Summary:During a survey of aminoacidopathies in the patients in various hospitals in the city, a Hindu joint family with increased urinary excretion of kynurenine, 3-hydroxykynurenine and xanthurenic acid was detected.
ISSN:0001-5652
1423-0062
DOI:10.1159/000152963