Yayın: A family with IgA nephropathy and hereditary lymphoedema praecox
| dc.contributor.author | Usta, Mehmet | |
| dc.contributor.author | Dilek, K. | |
| dc.contributor.author | Ersoy, Alparslan | |
| dc.contributor.author | Alper, Eray | |
| dc.contributor.author | Özbek, Serhat | |
| dc.contributor.author | Özdemir, Bülent | |
| dc.contributor.author | Fílíz, Gülaydan | |
| dc.contributor.author | Yavuz, Mahmut | |
| dc.contributor.author | Güllülü, Mustafa | |
| dc.contributor.author | Yurtkuran, Mustafa Abbas | |
| dc.contributor.buuauthor | Usta, Mehmet | |
| dc.contributor.buuauthor | Dilek, K. | |
| dc.contributor.buuauthor | ALPER, ERAY | |
| dc.contributor.buuauthor | ÖZBEK, SERHAT | |
| dc.contributor.buuauthor | ÖZDEMİR, BÜLENT | |
| dc.contributor.buuauthor | Fílíz, Gülaydan | |
| dc.contributor.buuauthor | YAVUZ, MAHMUT | |
| dc.contributor.buuauthor | GÜLLÜLÜ, MUSTAFA | |
| dc.contributor.buuauthor | Yurtkuran, Mustafa Abbas | |
| dc.contributor.department | Tıp Fakültesi | |
| dc.contributor.department | Nefroloji Ana Bilim Dalı | |
| dc.contributor.department | Nükleer Tıp Ana Bilim Dalı | |
| dc.contributor.department | Plastik ve Rekonstrüktif Cerrahi Ana Bilim Dalı | |
| dc.contributor.department | Kardiyoloji Ana Bilim Dalı | |
| dc.contributor.department | Patoloji Ana Bilim Dalı | |
| dc.contributor.scopusid | 7005030712 | |
| dc.contributor.scopusid | 6603823242 | |
| dc.contributor.scopusid | 35612977100 | |
| dc.contributor.scopusid | 7006827670 | |
| dc.contributor.scopusid | 7005245657 | |
| dc.contributor.scopusid | 7004168959 | |
| dc.contributor.scopusid | 6602693514 | |
| dc.contributor.scopusid | 7006244754 | |
| dc.contributor.scopusid | 6602684544 | |
| dc.contributor.scopusid | 7003389525 | |
| dc.date.accessioned | 2025-05-13T14:25:52Z | |
| dc.date.issued | 2002-05-30 | |
| dc.description.abstract | Usta 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.doi | 10.1046/j.1365-2796.2002.00976.x | |
| dc.identifier.endpage | 451 | |
| dc.identifier.issn | 0954-6820 | |
| dc.identifier.issue | 5 | |
| dc.identifier.scopus | 2-s2.0-0036096827 | |
| dc.identifier.startpage | 447 | |
| dc.identifier.uri | https://hdl.handle.net/11452/52928 | |
| dc.identifier.volume | 251 | |
| dc.indexed.scopus | Scopus | |
| dc.language.iso | en | |
| dc.relation.journal | Journal of Internal Medicine | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Immunoglobulin A nephropathy | |
| dc.subject | Hereditary lymphoedema | |
| dc.subject.scopus | Immunoglobulin A Nephropathy and Renal Outcomes | |
| dc.title | A family with IgA nephropathy and hereditary lymphoedema praecox | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.contributor.department | Tıp Fakültesi/Nefroloji Ana Bilim Dalı | |
| local.contributor.department | Tıp Fakültesi/Nükleer Tıp Ana Bilim Dalı | |
| local.contributor.department | Tıp Fakültesi/Plastik ve Rekonstrüktif Cerrahi Ana Bilim Dalı | |
| local.contributor.department | Tıp Fakültesi/Kardiyoloji Ana Bilim Dalı | |
| local.contributor.department | Tıp Fakültesi/Patoloji Ana Bilim Dalı | |
| local.indexed.at | Scopus | |
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