Congenital Stationary Night Blindness

Abstract

Objective

To examine the molecular causes of Schubert–Bornschein (S–B) congenital stationary night blindness (CSNB), clinically characterize in detail, and assess genotype–phenotype correlations for retinal function and structure.

Design

Retrospective, longitudinal, single-center case series.

Participants

One hundred twenty-two patients with S–B CSNB attending Moorfields Eye Hospital, United Kingdom.

Methods

All case notes, results of molecular genetic testing, and OCT were reviewed.

Main Outcome Measures

Molecular genetics, presenting complaints, rates of nystagmus, nyctalopia, photophobia, strabismus, color vision defects and spherical equivalent refraction (SER). Retinal thickness, outer nuclear layer (ONL) thickness, and ganglion cell layer + inner plexiform layer (GCL+IPL) thickness from OCT imaging.

Results

X-linked (CACNA1F and NYX) and autosomal recessive (TRPM1, GRM6, GPR179 and CABP4) genotypes were identified. The mean (± standard deviation) reported age of onset was 4.94 ± 8.99 years. Over the follow-up period, 95.9% of patients reported reduced visual acuity (VA), half had nystagmus, and 64.7% reported nyctalopia. Incomplete CSNB (iCSNB) patients more frequently had nystagmus and photophobia. Nyctalopia was similar for iCSNB and complete CSNB (cCSNB). Color vision data were limited but more defects were found in iCSNB. None of these clinical differences met statistical significance. There was no significant difference between groups in VA, with a mean of 0.46 logarithm of the minimum angle of resolution, and VA remained stable over the course of follow-up. Complete congenital stationary night blindness patients, specifically those with NYX and TRPM1 variants, were more myopic. CACNA1F patients showed the largest refractive variability, and the CABP4 patient was hyperopic. No significant differences were found in OCT structural analysis during the follow-up period.

Conclusions

Retinal structure in CSNB is stationary and no specific genotype–structure correlates were identified. Visual acuity seems to be relatively stable, with rare instances of progression.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.