Skip to main content
Log in

The incidence and presentation of dicarboxylic aciduria

  • Short Report
  • Published:
Journal of Inherited Metabolic Disease

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  • Bennett, M. J., Green, A., Pollitt, R. J. and Worthy, E. The routine investigation of urinary organic acids in selected paediatric patients: results over a 2 1/2-year period.Ann. Clin. Biochem. 21 (1984) 45–50

    Google Scholar 

  • Harpey, J.-P., Charpentier, C. and Paturneau-Jouas, M. Fatty acid β-oxidation defects and sudden infant death.Lancet 1 (1987) 163

    Google Scholar 

  • Pollitt, R. J., Losty, H. and Westwood, A. 3-Hydroxydicarboxylic aciduria: A distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance.J. Inher. Metab. Dis. 10 Suppl. 2 (1987) 266–269

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bennett, M.J., Worthy, E. & Pollitt, R.J. The incidence and presentation of dicarboxylic aciduria. J Inherit Metab Dis 10, 241–242 (1987). https://doi.org/10.1007/BF01800069

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01800069

Keywords

Navigation