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dc.contributor.authorYildiz L.
dc.contributor.authorAydin O.
dc.contributor.authorBoran C.
dc.contributor.authorKandemir B.
dc.contributor.authorAlper T.
dc.date.accessioned2020-06-21T09:16:13Z
dc.date.available2020-06-21T09:16:13Z
dc.date.issued1998
dc.identifier.issn1300-2996
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2875
dc.description.abstractAbdominal muscle deficiency, urinary tract abnormalities and cryptoorchidism are the three major features of the Prune-belly syndrome. Massive acites and intraabdominal urine accumination had produced abdominal wall atrophy. A functional or anatomic urethral obstruction may detect on cases. As an addition classic triad of Prune-belly syndrome our case has polydactily, cleft lip and palate. Chromosomal analysis could not be done our cases due to in utero exitus.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMultiple congenital anomaliesen_US
dc.subjectPrune-belly syndromeen_US
dc.titleA case of Prune-belly syndrome associated with multiple congenital anomaliesen_US
dc.title.alternativeMultipl konjenital anomalilerin eslik ettigi bir Prune-belly sendromu olgusuen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume15en_US
dc.identifier.issue4en_US
dc.identifier.startpage330en_US
dc.identifier.endpage334en_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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