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We describe a novel presentation of rod-cone dystrophy (RCD) phenocopying pigmented paravenous retinochoroidal atrophy associated with a mutation in CRX.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Case description:<\/jats:title>\n                    <jats:p>A 53-year-old man and his 48-year-old brother presented with a history of progressive vision loss and nyctalopia. Fundus examination revealed a bull\u2019s eye lesion with chorioretinal atrophy and intraretinal pigment migration, while spectral-domain optical coherence tomography (SD-OCT) demonstrated retinal thinning with outer retinal atrophy. On short-wavelength autofluorescence (SW-AF) imaging, an atypical paravenous pattern of atrophy with a surrounding hyperautofluorescent border was observed. Full-field electroretinogram (ffERG) revealed a rod-cone pattern of dysfunction. A heterozygous pathogenic variant, c.119G&gt;A:p.(Arg40Gln), in the CRX gene was identified in both brothers and segregated in their family.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>This case report broadens the currently known phenotypic presentations of CRX-associated retinopathy and suggests that mutations in CRX may be associated with pigmented paravenous retinochoroidal atrophy.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/1120672120957599","type":"journal-article","created":{"date-parts":[[2020,9,15]],"date-time":"2020-09-15T01:55:42Z","timestamp":1600134942000},"page":"NP235-NP239","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":10,"title":["A mutation in\n                    <i>CRX<\/i>\n                    causing pigmented paravenous retinochoroidal atrophy"],"prefix":"10.1177","volume":"32","author":[{"given":"Jin Kyun","family":"Oh","sequence":"first","affiliation":[{"name":"Jonas Children\u2019s Vision Care and Bernard & Shirlee Brown Glaucoma Laboratory, New York, NY, USA"},{"name":"State University of New York at Downstate Medical Center, Brooklyn, NY, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0118-4756","authenticated-orcid":false,"given":"Yan","family":"Nuzbrokh","sequence":"additional","affiliation":[{"name":"Jonas Children\u2019s Vision Care and Bernard & Shirlee Brown Glaucoma Laboratory, New York, NY, USA"},{"name":"Renaissance School of Medicine at Stony Brook University, Stony Brook, NY, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Winston","family":"Lee","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology, Columbia University Irving Medical Center, New York, NY, 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