Literature DB >> 29056504

Superior oblique myokymia.

Mia Zhang1, Aubrey Gilbert2, David G Hunter3.   

Abstract

Superior oblique myokymia (SOM) is a rare condition of unclear etiology. We discuss the history, etiology, clinical features, differential diagnoses, management, and prognosis of SOM. We conducted a meta-analysis of all 116 cases published since SOM was first described in 1906. The age at examination was 17-72 years (mean: 42 years.) There was a right-sided preponderance in 61% of cases (P < 0.02) that was statistically significant in females (63%, P < 0.04) but not in males (59%, P = 0.18). The pathophysiology of SOM may be neurovascular compression and/or ephaptic transmission. Although various pharmacological and surgical approaches to SOM treatment have been proposed, the rarity of the condition has made it impossible to conduct clinical trials evaluating the safety and efficacy of these approaches. Recently, topical beta blockers have managed SOM symptoms in a number of cases, including the first case treated with levobunolol. Systemic medications, strabismus surgery, and neurosurgery have been used to control symptoms, with strabismus surgery carrying a moderate risk of postoperative diplopia in downgaze. Although there is no established treatment for SOM, we encourage clinicians to attempt topical levobunolol therapy before considering systemic therapy or surgery.
Copyright © 2017 Elsevier Inc. All rights reserved.

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Keywords:  Harada-Ito procedure; monocular oscillopsia; superior oblique myokymia; superior oblique myokymia treatment; topical beta blocker; topical levobunolol

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Year:  2017        PMID: 29056504     DOI: 10.1016/j.survophthal.2017.10.005

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  1 in total

1.  Recurrent Superior Oblique Myokymia Treated by Distal Tendon Extirpation.

Authors:  Megan X Law; Creig S Hoyt; Jonathan C Horton
Journal:  J Neuroophthalmol       Date:  2019-09       Impact factor: 3.042

  1 in total

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