Cranial MRI findings in a case with Seckel syndrome

dc.contributor.authorAtalar, Mehmet Haydar
dc.date.accessioned2024-10-26T17:44:18Z
dc.date.available2024-10-26T17:44:18Z
dc.date.issued2018
dc.departmentSivas Cumhuriyet Üniversitesi
dc.description.abstractSeckel’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.doi10.7197/223.vi.417787
dc.identifier.endpage314
dc.identifier.issn1305-0028
dc.identifier.issue3
dc.identifier.startpage312
dc.identifier.trdizinid326298
dc.identifier.urihttps://doi.org/10.7197/223.vi.417787
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/326298
dc.identifier.urihttps://hdl.handle.net/20.500.12418/25192
dc.identifier.volume40
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.relation.ispartofCumhuriyet Tıp Dergisi (ELEKTRONİK)
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCerrahi
dc.titleCranial MRI findings in a case with Seckel syndrome
dc.typeArticle

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