Skip to main content

Advertisement

Log in

Ataxia with oculomotor apraxia type 2: not always an easy diagnosis

  • Letter to the Editor
  • Published:
Neurological Sciences Aims and scope Submit manuscript

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

References

  1. Anheim M, Monga B, Fleury M et al (2009) Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain 132:2688–2698

    Article  CAS  PubMed  Google Scholar 

  2. Nanetti L, Cavalieri S, Pensato V et al (2013) SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein. Orphanet J Rare Dis 8:123

    Article  PubMed Central  PubMed  Google Scholar 

  3. Schieving JH, de Vries M, van Vugt JM et al (2014) Alpha-fetoprotein, a fascinating protein and biomarker in neurology. Eur J Paediatr Neurol 18:243–248

    Article  CAS  PubMed  Google Scholar 

  4. Steinlin M (1998) Non-progressive congenital ataxias. Brain Dev 20:199–208

    Article  CAS  PubMed  Google Scholar 

  5. Synofzik M, Soehn AS, Gburek-Augustat J et al (2013) Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum. Orphanet J Rare Dis 8:41

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Conflict of interest

The authors declare that they have no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Maria Teresa Dotti.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mignarri, A., Tessa, A., Federico, A. et al. Ataxia with oculomotor apraxia type 2: not always an easy diagnosis. Neurol Sci 36, 1505–1507 (2015). https://doi.org/10.1007/s10072-015-2119-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10072-015-2119-z

Keywords

Navigation