| dc.contributor.author | Rizalar, R | |
| dc.contributor.author | Demirbilek, S | |
| dc.contributor.author | Bernay, F | |
| dc.contributor.author | Gurses, N | |
| dc.date.accessioned | 2020-06-21T11:31:55Z | |
| dc.date.available | 2020-06-21T11:31:55Z | |
| dc.date.issued | 1994 | |
| dc.identifier.issn | 0939-7248 | |
| dc.identifier.uri | https://doi.org/10.1055/s-2008-1066067 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/9938 | |
| dc.description | WOS: A1994MZ21700012 | en_US |
| dc.description | PubMed: 8199135 | en_US |
| dc.description.abstract | Congenital ''H-type'' urethrorectal communication with complete urethral stenosis is extremely rare in the pediatric population. The evaluation and surgical treatment of a ''H-type'' urethrorectal communication with complete urethral stenosis presenting in a 4-month-old infant is described. Additionally, he had a left renal agenesis and anal stenosis. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Hippokrates Verlag Gmbh | en_US |
| dc.relation.isversionof | 10.1055/s-2008-1066067 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | CONGENITAL URETHRORECTAL COMMUNICATION | en_US |
| dc.subject | URETHRAL STENOSIS | en_US |
| dc.subject | RENAL AGENESIS | en_US |
| dc.title | H-Type Urethrorectal Communication and Complete Urethral Stenosis With Unilateral Renal Agenesis | en_US |
| dc.type | note | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 4 | en_US |
| dc.identifier.issue | 1 | en_US |
| dc.identifier.startpage | 49 | en_US |
| dc.identifier.endpage | 50 | en_US |
| dc.relation.journal | European Journal of Pediatric Surgery | en_US |
| dc.relation.publicationcategory | Diğer | en_US |
