dc.contributor.author | Yildiz L. | |
dc.contributor.author | Aydin O. | |
dc.contributor.author | Boran C. | |
dc.contributor.author | Kandemir B. | |
dc.contributor.author | Alper T. | |
dc.date.accessioned | 2020-06-21T09:16:13Z | |
dc.date.available | 2020-06-21T09:16:13Z | |
dc.date.issued | 1998 | |
dc.identifier.issn | 1300-2996 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/2875 | |
dc.description.abstract | Abdominal 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.iso | tur | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Multiple congenital anomalies | en_US |
dc.subject | Prune-belly syndrome | en_US |
dc.title | A case of Prune-belly syndrome associated with multiple congenital anomalies | en_US |
dc.title.alternative | Multipl konjenital anomalilerin eslik ettigi bir Prune-belly sendromu olgusu | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 15 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 330 | en_US |
dc.identifier.endpage | 334 | en_US |
dc.relation.journal | Ondokuz Mayis Universitesi Tip Dergisi | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |