| dc.contributor.author | Akbalik M. | |
| dc.contributor.author | Bek K. | |
| dc.contributor.author | Karadeniz Ş. | |
| dc.contributor.author | Özkaya O. | |
| dc.contributor.author | Sağ Taşdöven Ç. | |
| dc.contributor.author | Baysal M.K. | |
| dc.date.accessioned | 2020-06-21T09:20:49Z | |
| dc.date.available | 2020-06-21T09:20:49Z | |
| dc.date.issued | 2006 | |
| dc.identifier.issn | 1300-2996 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/3372 | |
| dc.description.abstract | Primary hyperoxaluria is a rare, autosomal recessive inherited disease which is characterísed by recurrent urolithiasis, nephrocalcinosis and oxalate deposition throughout the body. We present here 45 days old male infant with early onset nephrocalcinosis and end stage renal disease due to primary hyperoxaluria. | en_US |
| dc.language.iso | tur | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Nephrocalcinosis | en_US |
| dc.subject | Primary hyperoxaluria | en_US |
| dc.subject | Renal failure | en_US |
| dc.title | A case of primary hyperoxaluria developing end stage renal failure in infancy | en_US |
| dc.title.alternative | Son dönem böbrek yetmezliği gelişen bir primer hiperokzalüri olgusu | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 23 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 65 | en_US |
| dc.identifier.endpage | 68 | en_US |
| dc.relation.journal | Ondokuz Mayis Universitesi Tip Dergisi | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
