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Research Article

Electroretinographic Findings in a Patient with Congenital Stationary Night Blindness Due to a Novel NYX Mutation

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Pages 167-173 | Received 23 Jul 2012, Accepted 15 Oct 2012, Published online: 04 Jan 2013
 

ABSTRACT

Purpose: To document a novel NYX gene mutation in a patient with X-linked complete congenital stationary night blindness and to describe this patient’s electroretinogram (ERG) characteristics.

Methods: ERGs were recorded from a 17-year-old male with a previously unreported NYX mutation (819G > A) that results in a missense codon change (Trp237Ter). ERGs were recorded in response to brief-flash stimuli, 6.33-Hz sawtooth flicker, and sinusoidal flicker ranging from 6.33–100 Hz. The omitted stimulus response (OSR) of the flicker ERG, which is thought to be generated within the ON-pathway, was also assessed.

Results: The patient’s single-flash responses were consistent with previously documented NYX ERG characteristics, including a high-luminance flash response that was electronegative under dark-adapted conditions and a square-like a-wave followed by an abnormally shaped positive potential under light-adapted conditions, both of which are consistent with an ON-pathway deficit. Further evidence for an ON-pathway deficit included: (1) ERGs to rapid-on sawtooth flicker in which b-wave amplitude was reduced more than a-wave amplitude, and (2) responses to sinusoidal flicker that lacked the normal amplitude minimum and phase inflection near 12 Hz, ERG characteristics that are like those of patients with other NYX mutations. Novel findings included a pronounced amplitude attenuation for sinusoidal flicker at frequencies above approximately 50 Hz and an absent OSR, suggesting ON-pathway dysfunction at high frequencies.

Conclusion: The substantial loss of ERG amplitude and apparent ON-pathway dysfunction at high temporal frequencies distinguish this patient with a Trp237Ter NYX mutation from those with other previously reported NYX mutations.

ACKNOWLEDGEMENTS

We thank Dr Beatrice Yue for assistance in genotyping the NYX patient.

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

Funding sources: This research was supported by National Institute of Health grants R00EY019510 (JJM), R01EY008301 (KRA), P30EY001792, a Center Grant from the Foundation Fighting Blindness (GAF), The Grant Healthcare Foundation (GAF), and an unrestricted departmental grant from Research to Prevent Blindness.

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