Hlas in Children With Minimal Change Disease and Other Types of Nephrotic Syndrome in the Southern Part of Turkey
dc.contributor.author | Karabay Bayazıt, Aysun | |
dc.contributor.author | Noyan, A. | |
dc.contributor.author | Bayazıt, Y. | |
dc.contributor.author | Özel, A. | |
dc.contributor.author | Anarat, A. | |
dc.date.accessioned | 2020-03-26T16:37:11Z | |
dc.date.available | 2020-03-26T16:37:11Z | |
dc.date.issued | 2001 | |
dc.department | Selçuk Üniversitesi | en_US |
dc.description.abstract | Karabay-Bayazit A, Noyan A, Bayazit Y, Ozel A,Anarat A. HLAs in children with minimal change disease and other types of nephrotic syndrome in the southern part of Turkey. Turk J Pediau 2001; 43: 24-28. The aim of this study was to investigate the human leukocyte antigen (HLA) profile of children with nephrotic syndrome in the southern part of Turkey. Seventy-eight children:with nephrotic syndrome were studied for the frequency of class I and class II human leukocyte antigens. Forty-seven of them were steroid sensitive nephrotic syndrome (minimal change disease-MCD) and 31 were other types of nephrotic syndrome. The results were compared with 133 healthy subjects for HLA groups. HLA B13, Cw5, Cw7, DR4 DR7, DRw10, Drw15(2) and DQ2 in the MCD group and HLA A31, B8, B13, B17, Cw2, Cw6, Cw7, DRw10 and DRw12 in the non-MCD group were found significantly increased when compared to healthy controls. MCD patients with frequent relapses had higher frequencies of both Cw6 and DR1 (p < 0.005) and MCD patients with infrequent relapses had a higher frequency of Cw7 (p < 0.05). In conclusion, HLA groups may help in the early diagnosis of these variants. | en_US |
dc.identifier.citation | Karabay Bayazıt, A., Noyan, A., Bayazıt, Y., Özel, A., Anarat, A., (2001). Hlas in Children With Minimal Change Disease and Other Types of Nephrotic Syndrome in the Southern Part of Turkey. Turkish Journal of Pediatrics, 43(1), 24-28. | |
dc.identifier.endpage | 28 | en_US |
dc.identifier.issn | 0041-4301 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 11297154 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 24 | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.12395/17556 | |
dc.identifier.volume | 43 | en_US |
dc.identifier.wos | WOS:000167689400004 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Turkish J Pediatrics | en_US |
dc.relation.ispartof | Turkish Journal of Pediatrics | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.selcuk | 20240510_oaig | en_US |
dc.subject | HLA | en_US |
dc.subject | nephrotic syndrome | en_US |
dc.subject | Turkish children | en_US |
dc.title | Hlas in Children With Minimal Change Disease and Other Types of Nephrotic Syndrome in the Southern Part of Turkey | en_US |
dc.type | Article | en_US |