Publication:
Partial agenesis of corpus callosum - Case study

dc.contributor.authorZamurović, M. (16065246600)
dc.contributor.authorAndjelic, S. (59577471700)
dc.date.accessioned2025-06-12T20:43:34Z
dc.date.available2025-06-12T20:43:34Z
dc.date.issued2014
dc.description.abstractAgenesis of the corpus callosum is an uncommon cerebral malformation usually of unknown etiology. It can be associated with other brain abnormalities, such as ventriculomegaly, or in combination with problems with other organs, such as congenital heart defect, as well as with chromosome anomalies. Diagnosis of this rare anomaly is important not only because of possible association with other developmental anomalies but also because of postnatal treatment and evaluation of children with this disorder. This paper presents prenatal diagnosis of partial agenesis of the posterior part of corpus callosum of a fetus detected in gestational week 33 by ultrasonography as an isolated developmental disorder, i.e., not accompanied by other morphological anomalies of the fetus or chromosome aberrations or other genetic defects.
dc.identifier.urihttps://doi.org/10.12891/ceog16032014
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84898843225&doi=10.12891%2fceog16032014&partnerID=40&md5=9a3cbed6f5827e4aa2d65240efe2b221
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/8882
dc.subjectCorpus callosum agenesis
dc.subjectFetal corpus callosum
dc.titlePartial agenesis of corpus callosum - Case study
dspace.entity.typePublication

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