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A family with IgA nephropathy and hereditary lymphoedema praecox

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dc.contributor.authorUsta, M
dc.contributor.authorDilek, Kamil
dc.contributor.authorErsoy, Ahmet
dc.contributor.authorAlper, E
dc.contributor.authorÖzbek, Serhat
dc.contributor.authorÖzdemir, Bülent
dc.contributor.authorFiliz, G
dc.contributor.authorYavuz, M
dc.contributor.authorGüllülü, Mustafa
dc.contributor.authorYurtkuran, Merih
dc.contributor.buuauthorUsta, M
dc.contributor.buuauthorDİLEK, KAMİL
dc.contributor.buuauthorErsoy, Ahmet
dc.contributor.buuauthorAlper, E
dc.contributor.buuauthorÖZBEK, SERHAT
dc.contributor.buuauthorÖZDEMİR, BÜLENT
dc.contributor.buuauthorFiliz, G
dc.contributor.buuauthorYavuz, M
dc.contributor.buuauthorGÜLLÜLÜ, MUSTAFA
dc.contributor.buuauthorYurtkuran, Merih
dc.contributor.departmentUludağ Üniversitesi Tıp Fakültesi/Nefroloji Bölümü
dc.contributor.departmentUludağ Üniversitesi Tıp Fakültesi/Nükleer Tıp Bölümü
dc.contributor.departmentUludağ Üniversitesi Tıp Fakültesi/Plastik ve Rekonstrüktif Cerrahi
dc.contributor.departmentUludağ Üniversitesi Tıp Fakültesi/Patoloji Anabilim Dallarından
dc.contributor.orcid0000-0003-3427-8337
dc.contributor.orcid0009-0001-9179-9107
dc.contributor.researcheridHYD-3798-2023
dc.contributor.researcheridCNY-9323-2022
dc.contributor.researcheridGXG-1656-2022
dc.contributor.researcheridCCY-8570-2022
dc.contributor.researcheridFTG-3544-2022
dc.contributor.researcheridJHE-3353-2023
dc.contributor.researcheridEVQ-8652-2022
dc.contributor.researcheridHJG-9929-2022
dc.contributor.researcheridJGS-9425-2023
dc.contributor.researcheridGLB-5791-2022
dc.date.accessioned2024-11-11T10:53:30Z
dc.date.available2024-11-11T10:53:30Z
dc.date.issued2002-05-01
dc.description.abstractImmunoglobulin A (IgA) nephropathy is the most common primary glomerulonephritis worldwide. The pathogenesis is still unknown and treatment has not yet been established. Rarely it can be associated with other disorders. Its association with hereditary lymphoedema is not reported before. We report four patients, a 60-year-old father, his two sons and his daughter, with hereditary lymphoedema. The family had nine members and in four of them lymphoedema was evident. The other members had neither lymphoedema nor IgA nephropathy. This is the first report of IgA nephropathy in association with hereditary lymphoedema.
dc.identifier.eissn1365-2796
dc.identifier.endpage451
dc.identifier.issn0954-6820
dc.identifier.issue5
dc.identifier.startpage447
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1046/j.1365-2796.2002.00976.x
dc.identifier.urihttps://hdl.handle.net/11452/47716
dc.identifier.volume251
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherWiley
dc.relation.journalJournal of Internal Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPathogenesis
dc.subjectLymphedema
dc.subjectHereditary lymphoedema
dc.subjectImmunoglobulin a nephropathy
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectMedicine, general & internal
dc.subjectGeneral & internal medicine
dc.titleA family with IgA nephropathy and hereditary lymphoedema praecox
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublication3483aae5-153f-4555-aa02-81efd2ace822
relation.isAuthorOfPublicationc45adcb3-b74a-4ea4-b2b2-8b0002084d1e
relation.isAuthorOfPublicationc653a7c1-4ead-46da-83e5-de7378a3726d
relation.isAuthorOfPublication47f5ec68-c479-4f62-9aed-37ba604a689c
relation.isAuthorOfPublication.latestForDiscovery3483aae5-153f-4555-aa02-81efd2ace822

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