Associated brain anomalies and clinical findings in corpus callosum dysgenesis
Küçük Resim Yok
Tarih
2003
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
PURPOSE: 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.
Açıklama
Anahtar Kelimeler
adolescent, adult, article, child, congenital malformation, corpus callosum, female, human, male, medical record, multiple malformation syndrome, nervous system malformation, nuclear magnetic resonance imaging, pathology, retrospective study, Turkey (republic), Abnormalities, Multiple, Adolescent, Adult, Child, Corpus Callosum, Female, Humans, Magnetic Resonance Imaging, Male, Medical Records, Nervous System Malformations, Retrospective Studies, Turkey
Kaynak
Tanisal ve girişimsel radyoloji : Tibbi Görüntüleme ve Girişimsel Radyoloji Dernegi yayin organi
WoS Q Değeri
Scopus Q Değeri
N/A
Cilt
9
Sayı
4
