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dc.contributor.authorAy, Larisa A.
dc.contributor.authorÖzkul, Bahattin
dc.contributor.authorAlataş, İbrahim
dc.contributor.authorUğurlar, Doğa
dc.contributor.authorGür Özcan, Seray G.
dc.contributor.authorAlizada, Orkhan
dc.contributor.authorÖzel, Şeyhmus K.
dc.date.accessioned2024-04-04T06:39:08Z
dc.date.available2024-04-04T06:39:08Z
dc.date.issued2023en_US
dc.identifier.citationAy, L. A., Özkul, B., Alataş, İ., Uğurlar, D., Özcan, S. G. G., Alizada, O., & Özel, Ş. K. (2023). Craniospinal MRI findings in spina bifida patients following fetoscopic, open and postnatal repair. GAZZETTA MEDICA ITALIANA ARCHIVIO PER LE SCIENZE MEDICHE, 182(11), 769-776. https://doi.org/https://orcid.org/0000-0003-3339-8329en_US
dc.identifier.issn1827-1812
dc.identifier.urihttps://hdl.handle.net/20.500.12900/333
dc.description.abstractBACKGROUND: Prenatal spina bifida repair and its clinical outcome are increasingly seen as topics of research even though early postnatal repair is routinely recommended for the treatment of spina bifida. The aim of this study was to evaluate the cranio-spinal MRI findings in spina bifida patients following prenatal and postnatal repair in a five-year follow-up study. METHODS: Hydrocephalus, Chiari malformation, malformations of cortical development, vertebral anomalies, syringohydromyelia, diastematomyelia, tethered cord were the parameters investigated in the cranio-spinal MRI of a group of nine patients that underwent prenatal (fetoscopic/open) or postnatal repair for spinal dysraphism. RESULTS: Follow-up MRI revealed no sign of Chiari malformation in patients that underwent prenatal repair. Hydrocephalus, gyral interdigitation and Chiari malformation were observed in the MRI of all of three patients that underwent postnatal repair. Heterotopia, polymicrogyria, and vermian hypoplasia were determined only in patients from postnatal repair group. In the fetoscopic repair group, scoliosis was seen in all patients, while vertebral segmentation, fusion anomalies, sacral dysgenesis were absent. In the prenatal open repair group vertebral segmentation was seen in one patient, scoliosis in two patients, while fusion anomalies and sacral dysgenesis were absent. Tethered cord syndrome was identified in all patients that underwent prenatal open repair and postnatal repair. CONCLUSIONS: In this category of patients larger and homogenous study groups combined with long term follow-up periods including evaluation of the cranial and spinal MRIs are necessary in order to have a better perspective over the consequences of each of these neurosurgical techniques.en_US
dc.language.isoengen_US
dc.publisherEDIZIONI MINERVA MEDICAen_US
dc.relation.isversionof10.23736/S0393-3660.23.05055-6en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSpinal disrafizmen_US
dc.subjectSpinal dysraphismen_US
dc.subjectFetoskopien_US
dc.subjectFetoscopyen_US
dc.subjectManyetik rezonans görüntülemeen_US
dc.subjectMagnetic resonance imagingen_US
dc.titleCraniospinal MRI findings in spina bifida patients following fetoscopic, open and postnatal repairen_US
dc.typearticleen_US
dc.departmentİstanbul Atlas Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.authoridhttps://orcid.org/0000-0003-3339-8329en_US
dc.contributor.institutionauthorÖzkul, Bahattin
dc.identifier.volume182en_US
dc.identifier.issue11en_US
dc.identifier.startpage769en_US
dc.identifier.endpage776en_US
dc.relation.journalGAZZETTA MEDICA ITALIANA ARCHIVIO PER LE SCIENZE MEDICHEen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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