Associated brain anomalies and clinical findings in corpus callosum dysgenesis

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dc.authorscopusid7006266098
dc.authorscopusid7003405757
dc.authorscopusid59026766300
dc.authorscopusid6701859321
dc.authorscopusid6603917376
dc.authorscopusid6506947472
dc.authorscopusid6508137336
dc.contributor.authorAlkan A.
dc.contributor.authorKutlu R.
dc.contributor.authorBaysal T.
dc.contributor.authorSigirci A.
dc.contributor.authorAltinok T.
dc.contributor.authorOrkan I.
dc.contributor.authorHallaç T.
dc.date.accessioned2024-08-04T20:01:01Z
dc.date.available2024-08-04T20:01:01Z
dc.date.issued2003
dc.departmentİnönü Üniversitesien_US
dc.description.abstractPURPOSE: The aim of this study was to evaluate the relationship between the types of the corpus callosum dysgenesis, the associated brain anomalies and clinical findings. MATERIALS AND METHODS: We analyzed the MR imaging findings in 169 patients with callosal dysgenesis. Corpus callosum dysgenesis was categorized into agenesis, hypogenesis and hypoplasia. The associated brain anomalies and clinical findings were evaluated. RESULTS: Associated brain anomalies were observed in 148 patients (87.5%). Twenty-one patients (12.4%) had isolated corpus callosum dysgenesis. Dysgenesis included agenesis in 22 (%13), hypogenesis in 46 (27.2%), and hypoplasia in 101 (59.7%) patients. The clinical findings were most commonly observed in patients with hypoplasia. CONCLUSION: The presence of corpus callosum dysgenesis is a strong indication of possible associated brain anomalies. Corpus callosum dysgenesis and associated brain anomalies should be investigated in children with developmental delay, seizures and microcephaly.en_US
dc.identifier.endpage417en_US
dc.identifier.issn1300-4360
dc.identifier.issue4en_US
dc.identifier.pmid14730948en_US
dc.identifier.scopus2-s2.0-1442333171en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage411en_US
dc.identifier.urihttps://hdl.handle.net/11616/91203
dc.identifier.volume9en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isotren_US
dc.relation.ispartofTanisal ve girişimsel radyoloji : Tibbi Görüntüleme ve Girişimsel Radyoloji Dernegi yayin organien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectadolescenten_US
dc.subjectadulten_US
dc.subjectarticleen_US
dc.subjectchilden_US
dc.subjectcongenital malformationen_US
dc.subjectcorpus callosumen_US
dc.subjectfemaleen_US
dc.subjecthumanen_US
dc.subjectmaleen_US
dc.subjectmedical recorden_US
dc.subjectmultiple malformation syndromeen_US
dc.subjectnervous system malformationen_US
dc.subjectnuclear magnetic resonance imagingen_US
dc.subjectpathologyen_US
dc.subjectretrospective studyen_US
dc.subjectTurkey (republic)en_US
dc.subjectAbnormalities, Multipleen_US
dc.subjectAdolescenten_US
dc.subjectAdulten_US
dc.subjectChilden_US
dc.subjectCorpus Callosumen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectMagnetic Resonance Imagingen_US
dc.subjectMaleen_US
dc.subjectMedical Recordsen_US
dc.subjectNervous System Malformationsen_US
dc.subjectRetrospective Studiesen_US
dc.subjectTurkeyen_US
dc.titleAssociated brain anomalies and clinical findings in corpus callosum dysgenesisen_US
dc.title.alternativeKorpus kallozum disgenezisine eşlik eden beyin anomalileri ve klinik bulgular.en_US
dc.typeArticleen_US

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