Multimodal imaging in Schubert-Bornschein congenital stationary night blindness

dc.contributor.authorParodi, Maurizio Battaglia
dc.contributor.authorArrigo, Alessandro
dc.contributor.authorRajabian, Firuzeh
dc.contributor.authorMansour, Ahmad Mohammed Farid Mahmoud
dc.contributor.authorMercuri, Stefano
dc.contributor.authorStarace, Vincenzo
dc.contributor.authorBordato, Alessandro
dc.contributor.authorManitto, Maria Pia
dc.contributor.authorMartina, Elisabetta
dc.contributor.authorBandello, Francesco Maria
dc.contributor.departmentOphthalmology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:09:03Z
dc.date.available2025-01-24T12:09:03Z
dc.date.issued2023
dc.description.abstractBackground: Schubert-Bornschein (SB) is the most common type of people with congenital stationary night blindness (CSNB). The aim of the study is to describe the optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) findings in patients with SB CSNB. Methods: Prospective, observational case series including three patients with genetically confirmed CSNB along with matched controls, who underwent complete ophthalmic examination and multimodal imaging. Results: On SD-OCT, a significant focal outer plexiform layer (OPL) thickening and a corresponding focal outer nuclear layer (ONL) thinning were identified in the macular area (p < 0.001). OCTA analysis overall showed decreased density of macular deep capillary plexus (mDCP) and macular choriocapillaris (mCC) (p = 0.008 and p = 0.033, respectively). DCP vessel density in the area corresponding to OPL thickening was significantly increased compared to the remaining retina (p < 0.001). Conclusion: SB CSNB is characterized by retinal vascular impairment, as detected on OCTA. © 2022 Taylor & Francis Group, LLC.
dc.identifier.doihttps://doi.org/10.1080/13816810.2022.2135108
dc.identifier.eid2-s2.0-85139949068
dc.identifier.pmid36226416
dc.identifier.urihttp://hdl.handle.net/10938/31978
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofOphthalmic Genetics
dc.sourceScopus
dc.subjectCongenital stationary night blindness
dc.subjectOptical coherence tomography angiography
dc.subjectSchubert-bornschein
dc.subjectFluorescein angiography
dc.subjectHumans
dc.subjectMultimodal imaging
dc.subjectNight blindness
dc.subjectNight blindness, congenital stationary
dc.subjectProspective studies
dc.subjectRetina
dc.subjectRetinal vessels
dc.subjectTomography, optical coherence
dc.subjectA wave
dc.subjectAdult
dc.subjectArticle
dc.subjectAutofluorescence imaging
dc.subjectB wave
dc.subjectBest corrected visual acuity
dc.subjectBlood vessel density
dc.subjectCacna1f gene
dc.subjectCentral macular thickness
dc.subjectChildhood
dc.subjectChoroid capillary layer
dc.subjectChoroidal thickness
dc.subjectClinical article
dc.subjectControlled study
dc.subjectDark adaptation
dc.subjectElectroretinogram
dc.subjectEye examination
dc.subjectGene
dc.subjectGenetic disorder
dc.subjectHigh throughput sequencing
dc.subjectHuman
dc.subjectImage quality
dc.subjectMale
dc.subjectMedical history
dc.subjectObservational study
dc.subjectPrognostic assessment
dc.subjectProspective study
dc.subjectRadial peripapillary capillary
dc.subjectRefraction error
dc.subjectRetinal outer nuclear layer
dc.subjectRetinal outer plexiform layer
dc.subjectRetinal thickness
dc.subjectSchubert bornschein congenital stationary night blindness
dc.subjectSlit lamp microscopy
dc.subjectSpectral domain optical coherence tomography
dc.subjectX chromosome
dc.subjectDiagnostic imaging
dc.subjectFluorescence angiography
dc.subjectGenetics
dc.subjectOptical coherence tomography
dc.subjectRetina blood vessel
dc.titleMultimodal imaging in Schubert-Bornschein congenital stationary night blindness
dc.typeArticle

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