Skip to main content

Ataxia-telangiectasia or neurologic Wilson’s disease: when strong family history becomes a diagnostic bias

This is a preview of subscription content, access via your institution.

References

  1. Dehkordy SF, Aghamohammadi A, Ochs HD, Rezaei N (2012) Primary immunodeficiency diseases associated with neurologic manifestations. J Clin Immunol 32:1–24

    PubMed  Article  Google Scholar 

  2. Moin M, Aghamohammadi A, Kouhi A, Tavassoli S, Rezaei N, Ghaffari SR, Gharagozlou M, Movahedi M, Purpak Z, Mirsaeid Ghazi B, Mahmoudi M, Farhoudi A (2007) Ataxia-telangiectasia in Iran: clinical and laboratory features of 104 patients. Pediatr Neurol 37(1):21–28

    PubMed  Article  Google Scholar 

  3. Lorincz MT (2010) Neurologic Wilson’s disease. Ann NY Acad Sci 1184:173–187

    PubMed  Article  CAS  Google Scholar 

  4. European Society for Immunodeficiencies. Diagnostic criteria for PID. http://www.esid.org/clinical-diagnostic-criteria-for-pid-73-0#Q1. Accessed 08 July 2012

  5. Roberts EA (2008) American Association for Study of Liver Diseases (AASLD). Diagnosis and treatment of Wilson disease: an update. Hepatology 47(6):2089–2111

    PubMed  Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Nima Rezaei.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Motamed, F., Benabbas, R., Ashrafi, M.R. et al. Ataxia-telangiectasia or neurologic Wilson’s disease: when strong family history becomes a diagnostic bias. Acta Neurol Belg 113, 195–196 (2013). https://doi.org/10.1007/s13760-012-0117-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13760-012-0117-y

Keywords

  • Autosomal Recessive Disease
  • Muscle Rigidity
  • Serum Ceruloplasmin
  • ATP7B Gene
  • Liver Copper