Skip to main content

Advertisement

Log in

Friedreich's ataxia presenting as adult-onset spastic paraparesis

  • Short communication
  • Published:
Neurogenetics Aims and scope Submit manuscript

ABSTRACT

We have studied a man with an atypical form of Friedreich's ataxia (FRDA), who presented at age 26 years with a 2-year history of unsteadiness and clumsiness. The predominant feature of his initial neurological examination was a spastic paraparesis, along with a mild distal weakness and hyperreflexia of the upper limbs. He also displayed limb ataxia. Frataxin GAA repeat sizes were 1040/690. This unusual FRDA presentation is not dissimilar to that of Acadian spastic ataxia.

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.

Institutional subscriptions

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: January 9, 1998 / Accepted: February 19, 1998

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gates, P., Paris, D., Forrest, S. et al. Friedreich's ataxia presenting as adult-onset spastic paraparesis. Neurogenetics 1, 297–299 (1998). https://doi.org/10.1007/s100480050045

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s100480050045

Navigation