Literature DB >> 1249684

Beta-methylcrotonic aciduria associated with lactic acidosis.

K Roth, R Cohn, J Yandrasitz, G Preti, P Dodd, S Segal.   

Abstract

A patient is described in whom lactic acidosis of very severe degree was found to coincide with the presence of beta-methylcrotonic acid and rho-hydroxyphenyllactic acid in urine in large amounts, while beta-hydroxyisovaleric acid was found to be a relatively minor excretion product. Beta-methylcrotonic acid is demonstrated, for the first time, to be present in blood and CSF. These findings are discussed in relation to the patients previously reported to have beta-methylcrotonylglycinuria and raise the possibility that our patient's organic aciduria may be secondary to acquired disease rather than to an inborn error of metabolism.

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Year:  1976        PMID: 1249684     DOI: 10.1016/s0022-3476(76)80987-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  19 in total

Review 1.  Holocarboxylase synthetase deficiency: 9-year follow-up of a patient on chronic biotin therapy and a review of the literature.

Authors:  A J Michalski; G T Berry; S Segal
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 2.  The biotin-dependent carboxylase deficiencies.

Authors:  B Wolf; G L Feldman
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

Review 3.  Enzyme studies in biotin-responsive disorders.

Authors:  K Bartlett; H K Ghneim; H J Stirk; H Wastell
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  [Reduction of biotin level as a possible factor in the mode of action of anticonvulsants (author's transl)].

Authors:  K H Krause; P Berlit; J P Bonjour
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1982

5.  Organic aciduria in hypoxic premature newborns simulating an inborn error of metabolism.

Authors:  J A Bakkeren; R C Sengers; J M Trijbels; P H Engels
Journal:  Eur J Pediatr       Date:  1977-12-30       Impact factor: 3.183

6.  Organic aciduria in neonatal multiple carboxylase deficiency.

Authors:  L Sweetman; W L Nyhan; N A Sakati; A Ohlsson; M S Mange; R B Boychuk; R Kaye
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

7.  Acetyl CoA carboxylase in cultured fibroblasts: differential biotin dependence in the two types of biotin-responsive multiple carboxylase deficiency.

Authors:  S Packman; N Caswell; M C Gonzalez-Rios; T Kadlecek; H Cann; D Rassin; C McKay
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

8.  Complementation studies of isovaleric acidemia and glutaric aciduria type II using cultured skin fibroblasts.

Authors:  B Dubiel; C Dabrowski; R Wetts; K Tanaka
Journal:  J Clin Invest       Date:  1983-11       Impact factor: 14.808

9.  Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.

Authors:  B J Burri; L Sweetman; W L Nyhan
Journal:  J Clin Invest       Date:  1981-12       Impact factor: 14.808

10.  Two forms of biotin-responsive multiple carboxylase deficiency.

Authors:  L Sweetman
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

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