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A family with IgA nephropathy and hereditary lymphoedema praecox

dc.contributor.authorUsta, Mehmet
dc.contributor.authorDilek, K.
dc.contributor.authorErsoy, Alparslan
dc.contributor.authorAlper, Eray
dc.contributor.authorÖzbek, Serhat
dc.contributor.authorÖzdemir, Bülent
dc.contributor.authorFílíz, Gülaydan
dc.contributor.authorYavuz, Mahmut
dc.contributor.authorGüllülü, Mustafa
dc.contributor.authorYurtkuran, Mustafa Abbas
dc.contributor.buuauthorUsta, Mehmet
dc.contributor.buuauthorDilek, K.
dc.contributor.buuauthorALPER, ERAY
dc.contributor.buuauthorÖZBEK, SERHAT
dc.contributor.buuauthorÖZDEMİR, BÜLENT
dc.contributor.buuauthorFílíz, Gülaydan
dc.contributor.buuauthorYAVUZ, MAHMUT
dc.contributor.buuauthorGÜLLÜLÜ, MUSTAFA
dc.contributor.buuauthorYurtkuran, Mustafa Abbas
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentNefroloji Ana Bilim Dalı
dc.contributor.departmentNükleer Tıp Ana Bilim Dalı
dc.contributor.departmentPlastik ve Rekonstrüktif Cerrahi Ana Bilim Dalı
dc.contributor.departmentKardiyoloji Ana Bilim Dalı
dc.contributor.departmentPatoloji Ana Bilim Dalı
dc.contributor.scopusid7005030712
dc.contributor.scopusid6603823242
dc.contributor.scopusid35612977100
dc.contributor.scopusid7006827670
dc.contributor.scopusid7005245657
dc.contributor.scopusid7004168959
dc.contributor.scopusid6602693514
dc.contributor.scopusid7006244754
dc.contributor.scopusid6602684544
dc.contributor.scopusid7003389525
dc.date.accessioned2025-05-13T14:25:52Z
dc.date.issued2002-05-30
dc.description.abstractUsta M, Dilek K, Ersoy A, Alper E, Özbek S, Özdemir B, Filiz G, Yavuz M, Güllülü M, Yurtkuran M (Uludaǧ University Medical School, Bursa, Turkey). A family with IgA nephropathy and hereditary lymphoedema praecox (Case Report). J Intern Med 2002; 251: 447-451. Immunoglobulin 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.doi10.1046/j.1365-2796.2002.00976.x
dc.identifier.endpage451
dc.identifier.issn0954-6820
dc.identifier.issue5
dc.identifier.scopus2-s2.0-0036096827
dc.identifier.startpage447
dc.identifier.urihttps://hdl.handle.net/11452/52928
dc.identifier.volume251
dc.indexed.scopusScopus
dc.language.isoen
dc.relation.journalJournal of Internal Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectImmunoglobulin A nephropathy
dc.subjectHereditary lymphoedema
dc.subject.scopusImmunoglobulin A Nephropathy and Renal Outcomes
dc.titleA family with IgA nephropathy and hereditary lymphoedema praecox
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Nefroloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Nükleer Tıp Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Plastik ve Rekonstrüktif Cerrahi Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Kardiyoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Patoloji Ana Bilim Dalı
local.indexed.atScopus
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relation.isAuthorOfPublication.latestForDiscovery1e873af6-0a6f-4d6b-81f9-a04478d62b26

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