Tc-99m DMSA scintigraphy in the diagnosis of renal anomalies: A Turner syndrome case

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dc.contributor.authorÖzdemir, Semra
dc.contributor.authorTan, Yusuf Ziya
dc.contributor.authorTopalo?lu, Naci
dc.contributor.authorSılan, Fatma
dc.contributor.authorTekin, Mustafa
dc.date.accessioned2025-01-27T19:04:33Z
dc.date.available2025-01-27T19:04:33Z
dc.date.issued2013
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractTurner syndrome (45, X0) is a chromosomal abnormality characterized by short stature, ovarian failure, streak gonad, hypertension, autoimmune thyroid disease, heart and renal anomalies. Here we report a case of Turner syndrome associated with crossed renal ectopia with fusion anomaly. A 8 year-old girl who had growth retardation and frequent urinary tract infection was investigated by Tc-99m DMSA scintigraphy. DMSA scan imaging showed crossed renal ectopia with fusion anomaly. The current case showed us once again that static renal Tc-99m DMSA scintigraphy imaging is an important diagnostic tool. It can not only determine renal cortical function but also can determine the congenital anomalies of the kidney including fusion anomalies. Copyright © 2013 by Türkiye Klinikleri.
dc.identifier.endpage40
dc.identifier.issn2146-8990
dc.identifier.issue1
dc.identifier.scopus2-s2.0-84875391042
dc.identifier.scopusqualityQ4
dc.identifier.startpage37
dc.identifier.urihttps://hdl.handle.net/20.500.12428/13992
dc.identifier.volume22
dc.indekslendigikaynakScopus
dc.language.isoen
dc.relation.ispartofTurkiye Klinikleri Pediatri
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250125
dc.subjectTechnetium Tc 99m dimercaptosuccinic acid; Turner syndrome
dc.titleTc-99m DMSA scintigraphy in the diagnosis of renal anomalies: A Turner syndrome case
dc.typeArticle

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