| dc.contributor.author | Kaya N. | |
| dc.contributor.author | Ketenci M. | |
| dc.contributor.author | Kosar A. | |
| dc.contributor.author | Ariturk N. | |
| dc.contributor.author | Akpolat I. | |
| dc.contributor.author | Altintop L. | |
| dc.contributor.author | Kahraman H. | |
| dc.date.accessioned | 2020-06-21T09:16:17Z | |
| dc.date.available | 2020-06-21T09:16:17Z | |
| dc.date.issued | 1998 | |
| dc.identifier.issn | 1300-4948 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/2888 | |
| dc.description.abstract | Gaucher's disease is a rare, chronically progressive, hereditary lipid storage disorder. Retinitis pigmentosa is a retinal dystrophia and there is no evidence in the literature of its link with Gaucher's disease. In our report, a case of retinitis pigmentosa with adult type Gaucher's disease is presented. | en_US |
| dc.language.iso | tur | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Gaucher's disease | en_US |
| dc.subject | Lipid storage disease | en_US |
| dc.subject | Retinitis pigmentosa | en_US |
| dc.title | Gaucher's disease and retinitis pigmentosa: A case report | en_US |
| dc.title.alternative | Gaucher hastaligi ve retinitis pigmentosa: Bir olgu sunumu | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 9 | en_US |
| dc.identifier.issue | 4 | en_US |
| dc.identifier.startpage | 377 | en_US |
| dc.identifier.endpage | 380 | en_US |
| dc.relation.journal | Turkish Journal of Gastroenterology | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
