Retinal findings in membranoproliferative glomerulonephritis

dc.contributor.authorMansour, Ahmad Mohammed Farid Mahmoud
dc.contributor.authorGonçalves de Lima, Luiz Henrique Soares
dc.contributor.authorArévalo, José Fernando
dc.contributor.authorAmaro, Miguel Hage
dc.contributor.authorLozano-López, Virginia
dc.contributor.authorBou Ghannam, Alaa S.
dc.contributor.authorChan, Errol Wei En
dc.contributor.departmentOphthalmology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:08:34Z
dc.date.available2025-01-24T12:08:34Z
dc.date.issued2017
dc.description.abstractPurpose: To assess the evolution of retinal findings in patients with membranoproliferative glomerulonephritis (MPGN) by funduscopy, intravenous fluorescein angiography and optical coherence tomography. Observations: Three women and one man were followed for a period of 1.5–37 years. Four patients (8 eyes) had drusen detected at first fundus exam at age 24, 29, 50 and 55. Three patients (6 eyes) had diffuse thickening of Bruch's membrane, and two patients (3 eyes) had detachment of the retinal pigment epithelium with serous retinal detachment. Drusen tended to widen over a period of 10-year follow-up in one case. Conclusions and importance: Drusen remain the ocular stigmata for MPGN occuring at an early age. The retinal disease is progressive with gradual thickening of Bruch's membrane and occurrence of retinal pigment epithelium detachment. © 2017 The Authors
dc.identifier.doihttps://doi.org/10.1016/j.ajoc.2017.06.011
dc.identifier.eid2-s2.0-85044441253
dc.identifier.urihttp://hdl.handle.net/10938/31842
dc.language.isoen
dc.publisherElsevier Inc
dc.relation.ispartofAmerican Journal of Ophthalmology Case Reports
dc.sourceScopus
dc.subjectDrusen
dc.subjectMacular degeneration
dc.subjectMembranoproliferative glomerulonephritis
dc.subjectRetinal pigment epithelial detachment
dc.titleRetinal findings in membranoproliferative glomerulonephritis
dc.typeArticle

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