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dc.contributor.authorCanbaz, B
dc.contributor.authorCiplak, N
dc.contributor.authorKaynar, MY
dc.contributor.authorKocer, N
dc.contributor.authorKuday, C
dc.contributor.authorErdincler, P
dc.date.accessioned2021-03-04T13:10:53Z
dc.date.available2021-03-04T13:10:53Z
dc.date.issued1998
dc.identifier.citationErdincler P., Kaynar M., Canbaz B., Kocer N., Kuday C., Ciplak N., "Iniencephaly: neuroradiological and surgical features - Case report and review of the literature", JOURNAL OF NEUROSURGERY, cilt.89, sa.2, ss.317-320, 1998
dc.identifier.issn0022-3085
dc.identifier.otherav_7b05ed69-8ac3-403a-a213-81a6cd4651e9
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/84248
dc.identifier.urihttps://doi.org/10.3171/jns.1998.89.2.0317
dc.description.abstractIniencephaly is a rare congenital anomaly characterized by spina bifida of the cervical vertebrae, fixed retroflexion of the head on the cervical spine, and occipital bone defect. There are only five reports of surviving patients with iniencephaly. The authors report the case of a newborn who presented with iniencephaly and an encephalocele that were surgically treated in our service. Neurological examination of the patient yielded normal results except for a moderate psychomotor retardation. The neuroradiological and surgical findings of the case suggested that the trigger of the anomaly was the occipital bone defect and rachischisis of the posterior vertebral arches.
dc.language.isoeng
dc.subjectCerrahi Tıp Bilimleri
dc.subjectTıp
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleIniencephaly: neuroradiological and surgical features - Case report and review of the literature
dc.typeMakale
dc.relation.journalJOURNAL OF NEUROSURGERY
dc.contributor.department, ,
dc.identifier.volume89
dc.identifier.issue2
dc.identifier.startpage317
dc.identifier.endpage320
dc.contributor.firstauthorID121181


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