| Literature DB >> 654914 |
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.Entities:
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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