Literature DB >> 1833200

Pellagra with colitis due to a defect in tryptophan metabolism.

P T Clayton1, N A Bridges, D J Atherton, P J Milla, M Malone, D A Bender.   

Abstract

A 9-year-old girl presented with a red scaly rash confined to sun-exposed areas which started at 2 years of age and had the appearance of pellagra. Investigation of urinary tryptophan metabolites following an oral tryptophan load, showed increased excretion of kynurenine and kynurenic acid but reduced excretion of 3-hydroxy-kynurenine, xanthurenic acid and N1-methyl nicotinamide. These results indicated a defect in the hydroxylation of kynurenine, an important reaction in the synthesis of the nicotinamide nucleotide coenzymes, NAD and NADP, from tryptophan. The patient went on to develop severe colitis and psychological changes. All her symptoms responded to treatment with nicotinamide.

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Year:  1991        PMID: 1833200     DOI: 10.1007/bf01958432

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  13 in total

1.  HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE.

Authors:  G M KOMROWER; V WILSON; J R CLAMP; R G WESTALL
Journal:  Arch Dis Child       Date:  1964-06       Impact factor: 3.791

2.  Molecular properties of L-kynurenine 3-hydroxylase from rat liver mitochondria.

Authors:  Y Nisimoto; F Takeuchi; Y Shibata
Journal:  J Biochem       Date:  1977-05       Impact factor: 3.387

3.  Rectal manifestations of pellagra.

Authors:  I Segal; L Ou Tim; A Demetriou; A Paterson; M Hale; M Lerios
Journal:  Int J Colorectal Dis       Date:  1986-10       Impact factor: 2.571

4.  Recurrent pellagra in Crohn's disease.

Authors:  M R Lucey
Journal:  Lancet       Date:  1982-09-04       Impact factor: 79.321

5.  Tryptophan metabolism. A hitherto unreported abnormality occurring in a family.

Authors:  J M Price; N Yess; R R Brown; A M Johnson
Journal:  Arch Dermatol       Date:  1967-05

6.  Pellagra: an analysis of 18 patients and a review of the literature.

Authors:  J L Spivak; D L Jackson
Journal:  Johns Hopkins Med J       Date:  1977-06

7.  Hydroxykynureninuria.

Authors:  G M Komrower; R Westall
Journal:  Am J Dis Child       Date:  1967-01

8.  Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.

Authors:  M A Salih; D A Bender; G M McCreanor
Journal:  Pediatrics       Date:  1985-11       Impact factor: 7.124

9.  Familial pellagra-like skin rash with neurological manifestations.

Authors:  E Freundlich; M Statter; S Yatziv
Journal:  Arch Dis Child       Date:  1981-02       Impact factor: 3.791

10.  Family exhibiting cerebellar-like ataxia, photosensitivity and shortness of stature - a new inborn error of tryptophan metabolism.

Authors:  D A Fenton; J D Wilkinson; P A Toseland
Journal:  J R Soc Med       Date:  1983-09       Impact factor: 18.000

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  3 in total

1.  Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase.

Authors:  M Christensen; M Duno; A M Lund; F Skovby; E Christensen
Journal:  J Inherit Metab Dis       Date:  2007-03-01       Impact factor: 4.750

Review 2.  Kynurenine Pathway of Tryptophan Metabolism: Regulatory and Functional Aspects.

Authors:  Abdulla A-B Badawy
Journal:  Int J Tryptophan Res       Date:  2017-03-15

3.  Alterations in serum amino acid concentrations in dogs with protein-losing enteropathy.

Authors:  Aarti Kathrani; Karin Allenspach; Andrea J Fascetti; Jennifer A Larsen; Edward J Hall
Journal:  J Vet Intern Med       Date:  2018-03-31       Impact factor: 3.333

  3 in total

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