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Published in: Neurological Sciences 6/2012

01-12-2012 | Case Report

Wernekink commissure syndrome: a rare midbrain syndrome

Authors: Huayan Liu, Lei Qiao, Zhiyi He

Published in: Neurological Sciences | Issue 6/2012

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Abstract

Wernekink commissure syndrome is a rare midbrain syndrome, which selectively destroys the Wernekink commissure involving the decussation of superior cerebellar peduncle in midbrain. This syndrome may display a clinical picture: bilateral cerebellar ataxia, eye movement disorders, and palatal tremor. We present two cases of the Wernekink commissure syndrome with acute onset of bilateral cerebellar dysfunction confirmed by magnetic resonance imaging. One patient presented internuclear ophthalmoplegia, but neither showed palatal tremor. It is notable that the bilateral cerebellar dysfunction may be ascribed to midbrain lesion involving the Wernekink commissure, and it may be the sole manifestation of the midbrain lesion.
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Metadata
Title
Wernekink commissure syndrome: a rare midbrain syndrome
Authors
Huayan Liu
Lei Qiao
Zhiyi He
Publication date
01-12-2012
Publisher
Springer Milan
Published in
Neurological Sciences / Issue 6/2012
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-012-0966-4

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