Skip to main content
Log in

Increased lactate in cerebrospinal fluid from 7 siblings in a family with mitochondrial myopathy and cerebellar ataxia

  • 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

  • Buchanan, D. N. and Thoene, J. C. Analysis of α-ketocarboxylic acids by ion exchange HPLC with UV and amperometric detection.J. Liq. Chromatogr. 224 (1981) 381–391

    Google Scholar 

  • Morgan-Hughes, J. A., Hayes, D. J., Clark, J. B., Landon, D. N., Swash, M., Stark, R. J. and Rudge, P. Mitochondrial encephalomyopathies, biochemical studies in two cases revealing defects in the respiratory chain.Brain 105 (1982) 553–582

    Google Scholar 

  • Sengers, R. C. A., Stadhouders, A. M. and Trijbels, J. M. F. Mitochondrial myopathies, clinical, morphological and biochemical aspects.Pediatrics 141 (1984) 192–207

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Borud, O., Torbergsen, T. & Mathiesen, E. Increased lactate in cerebrospinal fluid from 7 siblings in a family with mitochondrial myopathy and cerebellar ataxia. J Inherit Metab Dis 10, 400 (1987). https://doi.org/10.1007/BF01799985

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01799985

Keywords

Navigation