Literature DB >> 654914

Effects of thiamine in a patient with a variant form of branched-chian ketoaciduria.

M Duran, A G Tielens, S K Wadman, J C Stigter, W J Kleijer.   

Abstract

A boy with the intermediate variant of branched-chain ketoaciduria was studied. Treatment with an amino acid mixture was discontinued at the age of 7.5 years. Reintroduction of normal protein-containing foods precipitated the biochemical abnormalities, characteristic of MSUD, which were relieved by 10 mg thiamine/day. Adaptation to this regiment developed and thiamine intake was increased to 100 mg/day, later to 1 000 mg/day. The patient developed well and had no attacks of ketoacidosis. 1-14C-leucine degradation in intact fibroblasts was 15% of controls and did not increase upon addition of thiamine to the incubation medium.

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Year:  1978        PMID: 654914     DOI: 10.1111/j.1651-2227.1978.tb16336.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  4 in total

1.  Direct physical evidence for stabilization of branched-chain alpha-ketoacid dehydrogenase by thiamin pyrophosphate.

Authors:  S C Heffelfinger; E T Sewell; L J Elsas; D J Danner
Journal:  Am J Hum Genet       Date:  1984-07       Impact factor: 11.025

2.  Thiamin-responsive maple-syrup-urine disease: decreased affinity of the mutant branched-chain alpha-keto acid dehydrogenase for alpha-ketoisovalerate and thiamin pyrophosphate.

Authors:  D T Chuang; L S Ku; R P Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1982-05       Impact factor: 11.205

Review 3.  Animal models of maple syrup urine disease.

Authors:  K J Skvorak
Journal:  J Inherit Metab Dis       Date:  2009-03-09       Impact factor: 4.982

Review 4.  Thiamine-responsive inborn errors of metabolism.

Authors:  M Duran; S K Wadman
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

  4 in total

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