rss
Postgrad Med J 2004;80:363-365 doi:10.1136/pgmj.2003.015297
  • Case report

Dramatic levodopa responsiveness of dystonia in a sporadic case of spinocerebellar ataxia type 3

  1. R Nandagopal,
  2. S G K Moorthy
  1. Department of Neurology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India
  1. Correspondence to:
 Dr R Nandagopal
 Department of Neurology, Sri Venkateswara Institute of Medical Sciences, Tirupati-517 507, Andhra Pradesh, India; rnandagopalyahoo.com
  • Received 23 September 2003
  • Accepted 8 November 2003

Abstract

A genetically confirmed case of spinocerebellar ataxia type 3 (SCA 3), presenting with disabling foot dystonia, peripheral neuropathy, and minimal cerebellar signs is reported. The dystonia improved dramatically with levodopa treatment in the absence of additional parkinsonian feature. A trial of levodopa for dystonia in SCA 3 may be of therapeutic benefit, at least in the initial stage of the disease.

Footnotes

    Register for free content

    The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

    Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.