Skip Navigation


Brain Advance Access originally published online on November 7, 2003
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
127/2/280    most recent
awh030v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (4)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Migliaccio, A. A.
Right arrow Articles by Cremer, P. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Migliaccio, A. A.
Right arrow Articles by Cremer, P. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 127, No. 2, 280-293, 2004
© 2004 Guarantors of Brain
doi: 10.1093/brain/awh030

Cerebellar ataxia with bilateral vestibulopathy: description of a syndrome and its characteristic clinical sign

Americo A. Migliaccio, G. Michael Halmagyi, Leigh A. McGarvie and Phillip D. Cremer

Neurology Department, Royal Prince Alfred Hospital, Sydney, Australia

Correspondence to: Dr G. Michael Halmagyi, RPA Hospital, Camperdown, NSW 2050, Sydney, Australia E-mail: michael{at}icn.usyd.edu.au

We report four patients with the syndrome of cerebellar ataxia with bilateral vestibulopathy (CABV) and, using search coil oculography, we validate its characteristic clinical sign, namely impairment of the visually enhanced vestibulo-ocular reflex (VVOR) or doll’s head reflex. In our four patients, CABV began in the sixth decade of life; they are still ambulant and self-caring 8–20 years after onset. The cause of CABV in our four patients is unknown. None has a family history of cerebellar or vestibular disease; spinocerebellar ataxia (SCA) 1, 2, 3, 6, 7 and Friedreich’s ataxia were excluded by genetic testing. Three of the four have a sensory peripheral neuropathy but none has extrapyramidal or significant autonomic problems, and none has gluten sensitivity. We measured eye rotations in response to head-on-trunk head rotations and in response to head-and-trunk (en bloc) rotations. Horizontal smooth pursuit (SP), vestibulo-ocular reflex (VOR) and VVOR gains were measured in response to head rotations at 0.1, 0.3, 0.6 and 1.0 Hz. The optokinetic reflex (OKR) was tested by measuring optokinetic nystagmus slow phase velocity during constant 50°/s rotation of the subject in light. The results showed that CABV patients had impairment of all three compensatory eye movement reflexes, the VOR, the OKR and SP. During VVOR testing, as the frequency of head rotation increased from 0.1 to 1.0 Hz, eye velocity failed to match head velocity, gaze velocity increased, and gaze position errors developed, which were corrected with bursts of saccades, the basis of the clinical sign of an impaired VVOR.

Key Words: cerebellar ataxia; bilateral vestibulopathy; clinical test; vestibulo-ocular reflex; smooth pursuit; optokinetic

Abbreviations: BV= bilateral vestibulopathy; CA = cerebellar ataxia; CABV = cerebellar ataxia with bilateral vestibulopathy; MSA = multiple system atrophy; OKR = optokinetic reflex; SCA = spinocerebellar ataxia; SP = smooth pursuit; VOR = vestibulo-ocular reflex; VORS = visually suppressed vestibulo-ocular reflex; VVOR = visually enhanced vestibulo-ocular reflex

Received June 2, 2003. Revised August 28, 2003. Accepted September 1, 2003.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Neurol. Neurosurg. PsychiatryHome page
J N Wagner, M Glaser, T Brandt, and M Strupp
Downbeat nystagmus: aetiology and comorbidity in 117 patients
J. Neurol. Neurosurg. Psychiatry, June 1, 2008; 79(6): 672 - 677.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.