A Rare Midbrain Syndrome with Bilateral Cerebellar Ataxia and Isolated Superior Rectus Palsy: Wernekinck Commissure Syndrome

Khanghee Choi, Yong-Won Kim, Woochan Choi
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Abstract

Wernekinck commissure syndrome is a rare midbrain syndrome, usually resulting in selective destruction of the decussation of the superior cerebellar peduncle. This syndrome can present with symptoms such as bilateral cerebellar ataxia, ophthalmoplegia, and palatal tremor. Here, we report a 61-year-old female with acute onset of bilateral cerebellar ataxia and isolated superior rectus palsy diagnosed on Wernekinck commissure syndrome confirmed by magnetic resonance imaging.
伴有双侧小脑共济失调和孤立性直上肌麻痹的罕见中脑综合征:韦尔内金克 Commissure 综合征
Wernekinck commissure 综合征是一种罕见的中脑综合征,通常会导致小脑上部蝶鞍的选择性破坏。该综合征可表现为双侧小脑共济失调、眼肌麻痹和腭震颤等症状。在此,我们报告了一名 61 岁的女性患者,她急性发作双侧小脑共济失调和孤立性上直肌麻痹,经磁共振成像确诊为 Wernekinck commissure 综合征。
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