| dc.contributor.author | Aydin O. | |
| dc.contributor.author | Yildiz L. | |
| dc.contributor.author | Yilmaz D. | |
| dc.contributor.author | Kefeli M. | |
| dc.contributor.author | Erol H. | |
| dc.contributor.author | Yüksel C. | |
| dc.contributor.author | Kandemír B. | |
| dc.date.accessioned | 2020-06-21T09:23:25Z | |
| dc.date.available | 2020-06-21T09:23:25Z | |
| dc.date.issued | 2005 | |
| dc.identifier.issn | 1300-2996 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/3542 | |
| dc.description.abstract | Cardiac rhabdomyomas usually present early in life with a variety of symptoms including sudden death. Although primary cardiac tumors are rare, rhabdomyomas are seen most frequently in infancy and childhood. We present a female infant, who was dead in a short time after the discovery of a mediastinally mass and discuss its clinical and histopathological characteristics in the light of literature. | en_US |
| dc.language.iso | tur | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Cardiac | en_US |
| dc.subject | Rhabdomyoma | en_US |
| dc.subject | Sudden death | en_US |
| dc.title | Cardiac rhabdomyoma (case report) | en_US |
| dc.title.alternative | Kardiyak rabdomyom (olgu sunumu) | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 22 | en_US |
| dc.identifier.issue | 1 | en_US |
| dc.identifier.startpage | 37 | en_US |
| dc.identifier.endpage | 40 | en_US |
| dc.relation.journal | Ondokuz Mayis Universitesi Tip Dergisi | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
