Acquired oculomotor nerve paresis with cyclic spasms in a young woman, a rare subtype of neuromyotonia

Avi Gadoth*, Svetlana Kipervasser, Amos D. Korczyn, Miri Y. Neufeld, Anat Kesler

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

BACKGROUND: To report an unusual case of cyclic oculomotor nerve paresis and spasms, which developed 5 years following brain radiotherapy for cerebellar medulloblastoma. METHODS: Observational case report. RESULTS: The cyclic oculomotor nerve paresis and spasms resolved in our patient when treated with carbamazepine. However, because of severe photophobia and tearing, carbamazepine had to be discontinued leading to reappearance of the eye movement disorder. CONCLUSION: Cyclic oculomotor nerve paresis and spasms appear to be a delayed effect of radiotherapy and respond to carbamazepine therapy. It may be a rare form of ocular neuromyotonia.

Original languageEnglish
Pages (from-to)247-248
Number of pages2
JournalJournal of Neuro-Ophthalmology
Volume33
Issue number3
DOIs
StatePublished - Sep 2013

Fingerprint

Dive into the research topics of 'Acquired oculomotor nerve paresis with cyclic spasms in a young woman, a rare subtype of neuromyotonia'. Together they form a unique fingerprint.

Cite this