Skip to main content
Log in

Glycogen storage disease manifested as gout and myopathy: three case reports and literature review

  • Case Report
  • Published:
Clinical Rheumatology Aims and scope Submit manuscript

Abstract

Glycogen storage diseases (GSDs) are a group of congenital inherited metabolic diseases. They may present the symptoms of muscle and joint which may be misdiagnosed with some rheumatic diseases. We report three cases of GSDs in order to have a more clear recognition of the disease and to discuss the differential diagnosis.

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.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Chou JY, Matern D, Mansfield BC et al (2002) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex. Curr Mol Med 2(2):121–143

    PubMed  Google Scholar 

  2. Kishnani PS, Hwu WL, Mandel H et al (2006) A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr 148(5):671–676

    Article  PubMed  Google Scholar 

  3. Ausems MG, ten Berg K, Beemer FA (2000) Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families. Neuromuscul Disord 10(7):467–471

    Article  PubMed  Google Scholar 

  4. Winkel LP, Hagemans ML, van Doorn PA (2005) The natural course of non-classic Pompe’s disease: a review of 225 published cases. J Neurol 252(8):875–884

    Article  PubMed  Google Scholar 

  5. Kishnani PS, Nicolino M, Voit T et al (2006) Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease. J Pediatr 149(1):89–97

    Article  PubMed  CAS  Google Scholar 

  6. Van den Hout JM, Kamphoven JH, Winkel LP et al (2004) Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk. Pediatrics 113(5):e448–e457

    Article  PubMed  Google Scholar 

Download references

Disclosures

None

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Chun-de Bao.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhang, W., Bao, Cd., Gu, Yy. et al. Glycogen storage disease manifested as gout and myopathy: three case reports and literature review. Clin Rheumatol 27, 671–674 (2008). https://doi.org/10.1007/s10067-007-0798-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10067-007-0798-4

Keywords

Navigation