28
Views
1
CrossRef citations to date
0
Altmetric
ORIGINAL PAPER

Abnormal Electromyographic Findings in a Patient with Negative Scotopic Electroretinogram and Normal Dark Adaptation

, , , , , , & show all
Pages 1-7 | Accepted 01 Apr 2005, Published online: 26 Aug 2009
 

Abstract

Purpose: To present ocular and electromyographic findings in a patient with negative scotopic electroretinogram (ERG), reduced ON response, and normal dark adaptation. Patient: A 21-year-old Japanese female patient who complained of blurred vision. Her corrected visual acuity was 1.5 in each eye. Both fundi were normal. Dark adaptometry showed a normal pattern. Methods: The patient underwent ERG, contrast sensitivity testing, and electromyography (EMG). Results: The rod b-wave was reduced and delayed in the scotopic ERG. Scotopic bright flash response showed negative configuration. In the photopic responses to long flash, b-wave (ON response) was significantly reduced, while d-wave (OFF response) was within the normal range. The contrast sensitivity measurement showed high-frequency loss. Although she did not show muscle atrophy, weakness, or elevation of serum creatine kinase, the existence of myopathy was suggested by the EMG results. Conclusions: Dysfunctions of both rod and cone ON-bipolar cells were evident in the ERG findings. All ophthalmological results, except contrast sensitivity, were consistent with previous reports of diseases with an abnormal dystrophin gene condition: dystrophinopathy and its female carriers. The combination of negative ERG, reduced ON response, and normal dark adaptation might be a predictive indicator for muscle diseases such as dystrophinopathy and its female carriers.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.