Skip to main content
Log in

3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency

  • Case 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

  • Faull KF, Bolton PD, Halpern B, Hammond J, Danks DM (1976) The urinary organic acid profile associated with 3-hydroxy-3-methyl glutaric aciduria.Clin Chim Acta 73: 553–559.

    Google Scholar 

  • Ozand PT, Aqueel AA, Gascon G, Brismar J, Thomas E, Gleispach H (1991) 3-Hydroxy 3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudia Arabia:J Inher Metab Dis 14: 174–188.

    Google Scholar 

  • Wysocki SJ, Hähnel R (1986) 3-Hydroxy-3-methylglutaryl CoA lyase deficiency; a reviewJ Inher Metab Dis 9: 225–233.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Günel, M., Coşkun, T., Tokatli, A. et al. 3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency. J Inherit Metab Dis 16, 1062–1063 (1993). https://doi.org/10.1007/BF00711536

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00711536

Keywords

Navigation