Diaphragmatic myoclonus post cerebellar hemorrhage: a case report.

ABSTRACT:

Background

Diaphragmatic myoclonus is a rare motor disorder that affects muscle tone. It is characterized by involuntary movements of the abdominal wall and rhythmic, repetitive contractions of the accessory or respiratory muscles, all of which are innervated by the cervical nerve roots.

Case description

We reviewed the case of a 57-year-old male patient who underwent surgery for a left cerebellar hemorrhage. He exhibited persistent myoclonus in the palate, jaw, and thoracoabdominal region. Following treatment, there was a significant reduction in flutter amplitude in these areas.

Conclusion

The clinical rarity and variability of presentations often make diagnosis challenging and delayed. It is believed that this condition stems from abnormal excitation within the cen

SUBMITTER: Tan X 

PROVIDER: S-EPMC11363594 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature