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Wilms' tumor and associated malformations; Report of two cases with WAGR and Drash syndrome

dc.contributor.authorSalman, T
dc.contributor.authorCelik, A
dc.contributor.authorBoneval, C
dc.contributor.authorOzbey, H
dc.contributor.authorKapran, Y
dc.contributor.authorAksoyek, S
dc.date.accessioned2021-03-04T11:17:58Z
dc.date.available2021-03-04T11:17:58Z
dc.date.issued1996
dc.identifier.citationOzbey H., Boneval C., Kapran Y., Aksoyek S., Salman T., Celik A., "Wilms' tumor and associated malformations; Report of two cases with WAGR and Drash syndrome", EUROPEAN JOURNAL OF PEDIATRIC SURGERY, cilt.6, sa.3, ss.186-188, 1996
dc.identifier.issn0939-7248
dc.identifier.othervv_1032021
dc.identifier.otherav_71a191d7-81de-4896-806c-949806ab4437
dc.identifier.urihttp://hdl.handle.net/20.500.12627/78241
dc.identifier.urihttps://doi.org/10.1055/s-2008-1066505
dc.description.abstractThe combination of Wilms' tumor with aniridia, ambiguous genitalia/gonadoblastoma and mental retardation is defined as WAGR syndrome. The association with pseudohermaphroditism and nephropathy was also described as Drash syndrome. Here we report two cases with WAGR and Drash syndrome. The importance of early recognition and appropriate management of Wilms' tumor with those concurrent malformations is highlighted.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectCERRAHİ
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectCerrahi Tıp Bilimleri
dc.titleWilms' tumor and associated malformations; Report of two cases with WAGR and Drash syndrome
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF PEDIATRIC SURGERY
dc.contributor.department, ,
dc.identifier.volume6
dc.identifier.issue3
dc.identifier.startpage186
dc.identifier.endpage188
dc.contributor.firstauthorID117559


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