| dc.contributor.author | Ozyurek, Hamit | |
| dc.contributor.author | Kayacik, Ozlem Eroglu | |
| dc.contributor.author | Gungor, Olcay | |
| dc.contributor.author | Karagoz, Filiz | |
| dc.date.accessioned | 2020-06-21T15:14:23Z | |
| dc.date.available | 2020-06-21T15:14:23Z | |
| dc.date.issued | 2008 | |
| dc.identifier.issn | 0340-6199 | |
| dc.identifier.uri | https://doi.org/10.1007/s00431-007-0504-1 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/19393 | |
| dc.description | WOS: 000253573400021 | en_US |
| dc.description | PubMed: 17516083 | en_US |
| dc.description.abstract | We present the case of an 18-month-old boy with Hirschsprung's disease who had psychomotor retardation. His clinical and radiological findings were consistent with Joubert syndrome. The patient was the second case to show the association between Hirschsprung's disease and Joubert syndrome in the literature. As in our case, association of these entities by chance seems to be unlikely. Genetic analysis of new Joubert syndrome and Hirschsprung's disease patients may identify the candidate genes. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Springer | en_US |
| dc.relation.isversionof | 10.1007/s00431-007-0504-1 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Joubert syndrome | en_US |
| dc.subject | Hirschsprung's disease | en_US |
| dc.subject | neurocristopathy | en_US |
| dc.title | Rare association of Hirschsprung's disease and Joubert syndrome | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 167 | en_US |
| dc.identifier.issue | 4 | en_US |
| dc.identifier.startpage | 475 | en_US |
| dc.identifier.endpage | 477 | en_US |
| dc.relation.journal | European Journal of Pediatrics | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
