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Ophthalmic Genetics Volume 37, 2016 - Issue 4
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Review

Retinal disease in the C3 glomerulopathies and the risk of impaired vision

J. SavigeUniversity of Melbourne Department of Medicine, Melbourne Health and Northern Health, Royal Melbourne Hospital, Parkville, Victoria, Australia;Department of Nephrology, Royal Melbourne Hospital, Parkville, Victoria, AustraliaCorrespondence[email protected]
,
L. AmosUniversity of Melbourne Department of Medicine, Melbourne Health and Northern Health, Royal Melbourne Hospital, Parkville, Victoria, Australia
,
Frank IerinoDepartment of Nephrology, Austin Health, Heidelberg, Victoria, Australia
,
H. G. MackUniversity of Melbourne Department of Ophthalmology, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia
,
R. C. Andrew SymonsDepartment of Ophthalmology, Royal Melbourne Hospital, ParkvilleVictoria, Australia;University of Melbourne Department of Surgery, Royal Melbourne Hospital, ParkvilleVictoria, Australia
,
P. HughesDepartment of Nephrology, Royal Melbourne Hospital, Parkville, Victoria, Australia
,
K. NichollsDepartment of Nephrology, Royal Melbourne Hospital, Parkville, Victoria, Australia
&
D. ColvilleUniversity of Melbourne Department of Medicine, Melbourne Health and Northern Health, Royal Melbourne Hospital, Parkville, Victoria, Australia
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Pages 369-376 | Received 06 Aug 2015, Accepted 26 Sep 2015, Published online: 25 Feb 2016

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Read on this site (2)

Heather G Mack, Deborah J Colville, Phillip Harraka, Judith Anne Savige, Alessandro Invernizzi & Samantha Fraser-Bell. (2022) Retinal findings in glomerulonephritis. Clinical and Experimental Optometry 105:5, pages 474-486.
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Yan Chen, Deb Colville, Francesco Ierino, Andrew Symons & Judy Savige. (2018) Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy. Ophthalmic Genetics 39:2, pages 208-214.
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Articles from other publishers (24)

Ursula Greferath, Erica Fletcher, Judy Savige & Heather G. Mack. (2024) Drusen and Other Retinal Findings in People With IgA Glomerulonephritis. American Journal of Ophthalmology 257, pages 247-253.
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Vojtech Petr & Joshua M. Thurman. (2023) The role of complement in kidney disease. Nature Reviews Nephrology 19:12, pages 771-787.
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Martin Windpessl, Balazs Odler, Ingeborg M. Bajema, Duvuru Geetha, Marcus Säemann, Jiwon M. Lee, Augusto Vaglio & Andreas Kronbichler. (2023) Glomerular Diseases Across Lifespan: Key Differences in Diagnostic and Therapeutic Approaches. Seminars in Nephrology, pages 151435.
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Farid Shekarchian, Seyedeh Maryam Hosseini & Sahel Khazaei. (2023) Hypertensive retinopathy and Purtscher-like retinopathy in a child with complement 3 glomerulopathy. Journal of American Association for Pediatric Ophthalmology and Strabismus 27:5, pages 312-314.
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Taiga Inooka, Taro Kominami, Shunsuke Yasuda, Yoshito Koyanagi, Junya Ota, Satoshi Okado, Ryo Tomita, Yasuki Ito, Takeshi Iwase, Hiroko Terasaki, Koji M. Nishiguchi & Shinji Ueno. (2023) Assessment of factors affecting flicker ERGs recorded with RETeval from data obtained from health checkup screening. PLOS ONE 18:4, pages e0284686.
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Robyn H Guymer & Thomas G Campbell. (2023) Age-related macular degeneration. The Lancet 401:10386, pages 1459-1472.
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Aishwarya Ravindran, Lilian Monteiro Pereira Palma, Fernando C. Fervenza & Sanjeev Sethi. (2023) Overlap of C3 Glomerulopathy and Thrombotic Microangiopathy: A Case Series. Kidney International Reports 8:3, pages 619-627.
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Joshua M. Thurman & Richard A. Harrison. (2022) The susceptibility of the kidney to alternative pathway activation—A hypothesis. Immunological Reviews 313:1, pages 327-338.
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Keith Peters. (2022) Physiology and pathology of the C3 amplification cycle: A retrospective . Immunological Reviews 313:1, pages 217-224.
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P. Harraka, Tony Wightman, Sarah Akom, Kieran Sandhu, Deb Colville, Andrew Catran, David Langsford, Timothy Pianta, David Barit, Frank Ierino, Alison Skene, Heather Mack & Judy Savige. (2022) Increased retinal drusen in IgA glomerulonephritis are further evidence for complement activation in disease pathogenesis. Scientific Reports 12:1.
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E. Nicklason, Y. Ham, D. Ng, S. Glance, K. Abel, P. Harraka, H. Mack, D. Colville & J. Savige. (2022) Retinal drusen counts are increased in inflammatory bowel disease, and with longer disease duration, more complications and associated IgA glomerulonephritis. Scientific Reports 12:1.
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P. Harraka, H. Mack, D. Colville, D. Barit, D. Langsford, T. Pianta, F. Ierino & Judy Savige. (2022) Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesis. Scientific Reports 12:1.
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Ye Ji Ham, Eleanor Nicklason, Tony Wightman, Sarah Akom, Kieran Sandhu, Philip Harraka, Deb Colville, Andrew Catran, David Barit, David Langsford, Tim Pianta, Andrew Foote, Russell Buchanan, Heather Mack & Judy Savige. (2022) Retinal Drusen Are More Common and Larger in Systemic Lupus Erythematosus With Renal Impairment. Kidney International Reports 7:4, pages 848-856.
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Sarah de Jong, Elena B Volokhina, Anita de Breuk, Sara C Nilsson, Eiko K de Jong, Nicole C A J van der Kar, Bjorn Bakker, Carel B Hoyng, Lambert P van den Heuvel, Anna M Blom & Anneke I den Hollander. (2020) Effect of rare coding variants in the CFI gene on Factor I expression levels. Human Molecular Genetics 29:14, pages 2313-2324.
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Fernando Caravaca-Fontán, Laura Lucientes, Teresa Cavero & Manuel Praga. (2020) Update on C3 Glomerulopathy: A Complement-Mediated Disease. Nephron 144:6, pages 272-280.
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Judy Savige, Francesca Ariani, Francesca Mari, Mirella Bruttini, Alessandra Renieri, Oliver Gross, Constantinos Deltas, Frances Flinter, Jie Ding, Daniel P. Gale, Mato Nagel, Michael Yau, Lev Shagam, Roser Torra, Elisabet Ars, Julia Hoefele, Guido Garosi & Helen Storey. (2018) Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Pediatric Nephrology 34:7, pages 1175-1189.
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L. de-Pablo-Gómez-de-Liaño, I. Cañas Zamarra, J.I. Fernández-Vigo, M. Fernández Vidal, C. Navarro-Perea & T. Cavero Escribano. (2019) Retinal manifestations in patients with complement-mediated membranoproliferative glomerulonephritis. Archivos de la Sociedad Española de Oftalmología (English Edition) 94:2, pages 95-99.
Crossref
L. de-Pablo-Gómez-de-Liaño, I. Cañas Zamarra, J.I. Fernández-Vigo, M. Fernández Vidal, C. Navarro-Perea & T. Cavero Escribano. (2019) Manifestaciones retinianas en pacientes con glomerulonefritis membranoproliferativa mediada por complemento. Archivos de la Sociedad Española de Oftalmología 94:2, pages 95-99.
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Alan Cunningham & Ajay Kotagiri. (2018) A long history of dense deposit disease. BMC Ophthalmology 18:S1.
Crossref
Pranita Sahay, Ishan Pandya, Prafulla Kumar Maharana & Jeewan S Titiyal. (2018) Cloudy Cornea with Arcus Juvenilis in a Case of Dense Deposit Disease. BMJ Case Reports, pages bcr-2018-224545.
Crossref
Can Huzmeli, Mehmet Hadi Akkus & Ferhan Candan. (2018) C3 glomerulopathy disease. Cumhuriyet Medical Journal, pages 713-720.
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Valeria Kheir, Ali Dirani, Matthieu Halfon, Jean-Pierre Venetz, Georges Halabi & Yan Guex-Crosier. (2017) Multimodal imaging of retinal pigment epithelial detachments in patients with C3 glomerulopathy: case report and review of the literature. BMC Ophthalmology 17:1.
Crossref
Ahmad M. Mansour, Luiz H. Lima, J. Fernando Arevalo, Miguel Hage Amaro, Virginia Lozano, Alaa Bou Ghannam & Errol W. Chan. (2017) Retinal findings in membranoproliferative glomerulonephritis. American Journal of Ophthalmology Case Reports 7, pages 83-90.
Crossref
Alessandro Invernizzi, Laura dell'Arti, Gaia Leone, Daniela Galimberti, Elena Garoli, Gabriella Moroni, Alessandro Santaniello, Aniruddha Agarwal & Francesco Viola. (2017) Drusen-like Deposits in Young Adults Diagnosed With Systemic Lupus Erythematosus. American Journal of Ophthalmology 175, pages 68-76.
Crossref

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