Journal of Inherited Metabolic Disease

, Volume 10, Supplement 2, pp 266–269 | Cite as

3-Hydroxydicarboxylic aciduria: A distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance

  • R. J. Pollitt
  • H. Losty
  • A. Westwood
Short Communication

Keywords

Public Health Internal Medicine Metabolic Disease Distinctive Type Diagnostic Significance 

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References

  1. Greter, J., Lindstedt, S., Seeman, H. and Steen, G. 3-Hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis.Clin. Chem. 26 (1980) 261–265PubMedGoogle Scholar
  2. Mortensen, P. B. Dicarboxylic acids and the lipid metabolism.Dan. Med. Bull. 31 (1980) 121–145Google Scholar
  3. Riudor, E., Ribes, A., Boronat, M., Sabado, C., Dominguez, C. and Ballabriga, A. A new case of C6–C14 dicarboxylic aciduria with favourable evolution.J. Inher. Metab. Dis. 9 Suppl. 2 (1986) 297–299PubMedGoogle Scholar
  4. Rocchiccioli, F., Aubourg, P. and Bougnères, P. F. Medium-and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleucodystrophy.Pediatr. Res. 20 (1986) 62–66PubMedGoogle Scholar

Copyright information

© SSIEM and MTP Press Limited 1987

Authors and Affiliations

  • R. J. Pollitt
    • 1
  • H. Losty
    • 2
  • A. Westwood
    • 2
  1. 1.University Department of Psychiatry and Regional Neonatal Screening LaboratoryMiddlewood HospitalSheffieldUK
  2. 2.Department of Paediatric BiochemistryRoyal Hospital for Sick ChildrenEdinburghUK

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