Cranial MRI findings in a case with Seckel syndrome
dc.contributor.author | Atalar, Mehmet Haydar | |
dc.date.accessioned | 2024-10-26T17:44:18Z | |
dc.date.available | 2024-10-26T17:44:18Z | |
dc.date.issued | 2018 | |
dc.department | Sivas Cumhuriyet Üniversitesi | |
dc.description.abstract | Seckel’s syndrome (SS) is a rare, heterogeneous form of primordial dwarfism. The presence of mental retardation andneurologic signs is one of the peculiar features of this syndrome. We herein present the cranial MR findings in a childpatient with Seckel's syndrome. | |
dc.identifier.doi | 10.7197/223.vi.417787 | |
dc.identifier.endpage | 314 | |
dc.identifier.issn | 1305-0028 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 312 | |
dc.identifier.trdizinid | 326298 | |
dc.identifier.uri | https://doi.org/10.7197/223.vi.417787 | |
dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/326298 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/25192 | |
dc.identifier.volume | 40 | |
dc.indekslendigikaynak | TR-Dizin | |
dc.language.iso | en | |
dc.relation.ispartof | Cumhuriyet Tıp Dergisi (ELEKTRONİK) | |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Cerrahi | |
dc.title | Cranial MRI findings in a case with Seckel syndrome | |
dc.type | Article |