Evidence map›Paper›PMID 41995403›Full record

ArticleRetinal cases & brief reports2025

MIDPERIPHERAL RETINAL THICKENING ON WIDEFIELD OPTICAL COHERENCE TOMOGRAPHY IN A PATIENT WITH A MUTATION IN THE NR2E3 GENE.

Jan Willem R Pott, E Angela Huiskamp, Joke B G M Verheij

Abstract readCase Reports
In one paragraph

Article in Retinal cases & brief reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jan Willem R PottDepartments of Ophthalmology, and.ORCID 0000-0003-0860-1356
E Angela HuiskampDepartments of Ophthalmology, and.
Joke B G M VerheijGenetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo report typical retinal findings in a girl with the presumed diagnosis of enhanced S-cone syndrome, attributed to the presence of a homozygous likely pathogenic variation in the NR2E3 gene.

methodsA retrospective case report with multimodal imaging studies.

resultsWidefield OCT examination at the age of 11 showed increased thickening of the midperipheral retina. In the area of retinal thickening, the delineation of retinal architecture was coarse and photoreceptor outer segments thinned and disrupted. The retinal pigment epithelium appeared to be normal on autofluorescence imaging. In retrospect, the retinal thickening was already apparent on conventional OCT at the age of 3.

conclusionWidefield OCT is a valuable new tool in assessing typical retinal abnormalities in patients with NR2E3 mutations, by showing an abnormal but very characteristic thickening of the midperipheral retina.

Indexed as

Eye Diseases, HereditaryNight BlindnessOrphan Nuclear ReceptorsRetinaRetinal DegenerationTomography, Optical CoherenceVision DisordersChildFemaleHumansMutationRetrospective StudiesNR2E3 protein, humanOrphan Nuclear Receptorsenhanced S-cone syndromeNR2E3widefield OCT

Identifiers

PMID41995403
PMCPMC12382738

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.