Journal of Inherited Metabolic Disease

, Volume 26, Issue 7, pp 711–712 | Cite as

Case Report: Rhabdomyolysis in Glutaric Aciduria Type I

  • S. L. Chow
  • C. Rohan
  • A. A. M. MorrisEmail author


Recurrent rhabdomyolysis has previously been reported in one patient with glutaric aciduria type I. We report rhabdomyolysis in a second, unrelated patient, suggesting that there may be a specific association with this metabolic disorder.


Carnitine Creatine Supplementation Glutaric Aciduria Type Acetylcarnitine Generalize Dystonia 
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  1. Das AM, Lucke T, Ullrich K (2003) Glutaric aciduria I: creatine supplementation restores creatine phosphate levels in mixed cortex cells from rat incubated with 3-hydroxyglutarate. Mol Genet Metab 78: 108–111.PubMedCrossRefGoogle Scholar
  2. Ullrich K, Flott-Rahmel B, Schluff P, et al (1999) Glutaric aciduria type I: pathomechanisms of neurodegeneration. J Inherit Metab Dis 22: 392–403.PubMedCrossRefGoogle Scholar
  3. Wilson CJ, Collins JE, Leonard JV (1999) Recurrent rhabdomyolysis in a child with glutaric aciduria type I. J Inherit Metab Dis 22: 663–664.PubMedCrossRefGoogle Scholar

Copyright information

© Kluwer Academic Publishers 2003

Authors and Affiliations

  1. 1.Metabolic UnitLondon
  2. 2.Department of PaediatricsChase Farm HospitalLondonUK

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