Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency

Published:1993 Issue:5 Volume:16 Page:851-856
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Bergoffen J.,Kaplan P.,Hale D. E.,Bennett M. J.,Berry G. T.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF00714277

Reference12 articles.

1. Bennett MJ, Ragni MC, Head I et al (1992) Comparison of post-mortem urinary and vitreous humour organic acids.Ann Clin Biochem 29: 541?545.

2. Dosman J, Crawhall JC, Klassen GA et al (1974) Urinary excretion of C6?C10 dicarboxylic acids in glycogen storage disease types I and III.Clin Chim Acta 51: 93?101.

3. Greter J, Lindstedt S, Seeman H et al (1980) 3-Hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis.Clin Chem 26: 261?265.

4. Hagenfeldt L, von Dobeln U, Holme E et al (1990)l-3-Hydroxydicarboxylic aciduria ? a fatty acid oxidation defect with severe prognosis.J Pediatr 116: 387?392.

5. Hale DE, Thorpe C, Braat K et al (1990) Thel-3-hydroxyacyl-CoA dehydrogenase deficiency.Prog Clin Biol Res 321: 503?510.

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