Publication:
Nephrotic Syndrome in Childhood: Retrospective Evaluation of 230 Cases

dc.authorscopusid6603873361
dc.authorscopusid7003707808
dc.authorscopusid6602111071
dc.authorscopusid7004842978
dc.authorscopusid7003539720
dc.contributor.authorVan, A.
dc.contributor.authorİşlek, I.
dc.contributor.authorDaǧdemir, A.
dc.contributor.authorKoçak, H.
dc.contributor.authorKüçüködük, S.
dc.date.accessioned2025-12-11T02:04:44Z
dc.date.issued2001
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Van] A., Tip Fakultesi, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [İşlek] İsmail, Tip Fakultesi, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Daǧdemir] Ayhan, Tip Fakultesi, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Koçak] Hulusi, Tip Fakultesi, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Küçüködük] Şükrü, Tip Fakultesi, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractIn this study, we evaluated 230 children (0 to 17 years old) with nephrotic syndrome (NS) who admitted to the Department of Pediatrics of Ondokuz Mayas University between January 1986 to December 1998, retrospectively. The diagnostic criteria of International Study of Kidney Diseases of Children (ISKDC) were used to define the patients in this study. Patients were classified into two groups according to etiology as primary and secondary NS. Clinical and laboratory findings of all cases were examined. It is observed that 77.8% of the cases had primary and 17.4% had secondary NS, 4.8% of them could not be classified, 39.1% of the patients were female and 60.9% of them were male. Female/male ratio was 1/1.6. Steroid responsive cases consisted 77.8% of the cases with minimal change NS [MCNS), 51% of the patients with steroid responsive MCNS developed one or more relapses. Among the relapses, rare and frequent relapses were 29.4% and 10.7%, respectively. 3.9% of the patients with MCNS were steroid dependent. Amyloidosis was diagnosed in 27 patients and it was the most common cause of secondary NS, The most frequent complication was infection. In 230 patients, 57.4% went to remission, 5.6% died and 10.4% progressed to chronic renal failure. These findings were evaluated according to age, sex, etiology, response to treatment, prognosis and compared with national data and the literature.en_US
dc.identifier.endpage79en_US
dc.identifier.issn1300-2996
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-0034923304
dc.identifier.scopusqualityN/A
dc.identifier.startpage71en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/47659
dc.identifier.volume18en_US
dc.identifier.wosqualityN/A
dc.language.isotren_US
dc.relation.ispartofOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmyloidosisen_US
dc.subjectChildhooden_US
dc.subjectNephrotic Syndromeen_US
dc.titleNephrotic Syndrome in Childhood: Retrospective Evaluation of 230 Casesen_US
dc.title.alternativeÇocukluk Çağı Nefrotik Sendromu: 230 Olgunun Değerlendirilmesien_US
dc.typeArticleen_US
dspace.entity.typePublication

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