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dc.contributor.authorAlkan, Ozlem
dc.contributor.authorKizilkilic, Osman
dc.contributor.authorYildirim, Tulin
dc.date.accessioned2021-03-04T07:57:09Z
dc.date.available2021-03-04T07:57:09Z
dc.date.issued2009
dc.identifier.citationAlkan O., Kizilkilic O., Yildirim T., "Malformations of the Midbrain and Hindbrain: A Retrospective Study and Review of the Literature", CEREBELLUM, cilt.8, sa.3, ss.355-365, 2009
dc.identifier.issn1473-4222
dc.identifier.otherav_60bbc6a5-99ae-469a-8f2c-68eeaaede44d
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/67486
dc.identifier.urihttps://doi.org/10.1007/s12311-009-0104-x
dc.description.abstractWe report the results of a retrospective analysis of radiological and clinical findings in 45 cases of midbrain-hindbrain anomalies and review recent advances in embryology and molecular neurogenetics. Among 45 patients with midbrain-hindbrain malformations, 16 cases of molar tooth malformation, 12 of cerebellar hypoplasia, ten of posterior fossa cyst and cerebellar vermian hypoplasia, three of rhombencephalosynapsis, two of Fukuyama congenital muscular dystrophy and two cases of isolated cerebellar dysplasia were identified. Twenty-six patients presented with motor-mental retardation, which was the most common clinical finding. Eleven patients were born to consanguineous parents. The correct diagnosis of cerebellar malformation is important for determining prognosis, the risk of recurrence and the need for genetic counselling. Integrated classification of malformations based on morphology, embryology and molecular neurogenetics may be useful.
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri
dc.titleMalformations of the Midbrain and Hindbrain: A Retrospective Study and Review of the Literature
dc.typeMakale
dc.relation.journalCEREBELLUM
dc.contributor.departmentBaşkent Üniversitesi , ,
dc.identifier.volume8
dc.identifier.issue3
dc.identifier.startpage355
dc.identifier.endpage365
dc.contributor.firstauthorID193257


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