Abstract

BackgroundWernekink commissure syndrome causes a peculiar combination of internuclear ophthalmoplegia, dysarthria, and delayed-onset palatal myoclonus. Palatal myoclonus is thought to be secondary to delayed hypertrophic degeneration of the bilateral inferior olivary nuclei secondary to involvement of bilateral dentatoolivary tract. We describe a case of a patient with early-onset palatal myoclonus.Case presentationA 53-year-old Caucasian man with several vascular risk factors presented to our emergency room with slurred speech, double vision, difficulty with swallowing and walking, and rhythmic contractions of the soft palate. Brain magnetic resonance imaging showed an acute infarct of the right caudal midbrain and an old infarct of the right medulla. We hypothesize that the cause of early palatal myoclonus in our patient was a two-hit mechanism with degeneration of the right olivary nucleus resulting from prior right medullary lacunar stroke with the new infarct affecting the dentato-rubro-olivary tract on the left side, causing bilateral dysfunction initiating palatal myoclonus.ConclusionsWernekink commissure syndrome with palatal myoclonus at onset suggests the presence of a prior ischemic insult in the medulla. Careful examination is important to identification of this presentation.

Highlights

  • Wernekink commissure syndrome causes a peculiar combination of internuclear ophthalmoplegia, dysarthria, and delayed-onset palatal myoclonus

  • Wernekink commissure syndrome with palatal myoclonus at onset suggests the presence of a prior ischemic insult in the medulla

  • Wernekink commissure syndrome is a rare midbrain syndrome characterized by bilateral cerebellar ataxia, internuclear ophthalmoplegia, dysarthria, and delayedonset palatal myoclonus or Holmes tremor secondary to a stroke in the paramedian caudal midbrain region [1,2,3,4]

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Summary

Conclusions

Wernekink commissure syndrome is one of the rare paramedian caudal midbrain stroke syndromes that can cause tetra-ataxia, internuclear ophthalmoplegia, dysarthria, variable eye movement disorders, Holmes tremor, and delayed palatal myoclonus.

Background
Discussion

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