dc.contributor.author | GOKALP, A | |
dc.contributor.author | GULTEKIN, EY | |
dc.date.accessioned | 2019-07-27T12:10:23Z | |
dc.date.accessioned | 2019-07-28T10:38:54Z | |
dc.date.available | 2019-07-27T12:10:23Z | |
dc.date.available | 2019-07-28T10:38:54Z | |
dc.date.issued | 1993 | |
dc.identifier.issn | 0041-4301 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/11965 | |
dc.description | WOS: A1993MB63800014 | en_US |
dc.description | PubMed ID: 8249197 | en_US |
dc.description.abstract | A 14-day-old male infant with megalourethra is presented because of the rarity of the anomaly and its association with prune-belly syndrome. The lax, wrinkled appearance of the abdomen, bilateral cryptorchidism and severe dilatation of the urinary system are features included in the classic triad of the prune-belly syndrome. Our patient had the scaphoid variety of megalourethra since the penis appeared elongated and floppy in the fusiform form. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | TURKISH J PEDIATRICS | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | MEGALOURETHRA | en_US |
dc.subject | PRUNE-BELLY SYNDROME | en_US |
dc.subject | CONGENITAL ANOMALY | en_US |
dc.title | MEGALOURETHRA ASSOCIATED WITH PRUNE-BELLY SYNDROME | en_US |
dc.type | other | en_US |
dc.relation.journal | TURKISH JOURNAL OF PEDIATRICS | en_US |
dc.identifier.volume | 35 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.endpage | 153 | en_US |
dc.identifier.startpage | 151 | en_US |
dc.relation.publicationcategory | Diğer | en_US |