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Prenatal diagnosis of agenesis of corpus callosum: what is the neurodevelopmental outcome?

Authors

  • PISANI FRANCESCO,

    Corresponding author
    1. 1Developmental Neuropsychiatric Unit and 2Department of Gynaecology, Obstetrics and Neonatal Medicine, University of Parma, Parma, Italy
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  • 1 BIANCHI MARIA-EDGARDA,

    1. 1Developmental Neuropsychiatric Unit and 2Department of Gynaecology, Obstetrics and Neonatal Medicine, University of Parma, Parma, Italy
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  • 1 PIANTELLI GIOVANNI,

    1. 1Developmental Neuropsychiatric Unit and 2Department of Gynaecology, Obstetrics and Neonatal Medicine, University of Parma, Parma, Italy
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  • 2 GRAMELLINI DANDOLO,

    1. 1Developmental Neuropsychiatric Unit and 2Department of Gynaecology, Obstetrics and Neonatal Medicine, University of Parma, Parma, Italy
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  • and 2 BEVILACQUA GIULIO 2

    1. 1Developmental Neuropsychiatric Unit and 2Department of Gynaecology, Obstetrics and Neonatal Medicine, University of Parma, Parma, Italy
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Francesco Pisani, Developmental Neuropsychiatric Unit, University of Parma, Via Gramsci 14, 43100 Parma, Italy. Email: francesco.pisani@unipr.it

Abstract

Background: Corpus callosum is the largest cerebral commissure that connects neocortical areas. Agenesis of corpus callosum (ACC) can be partial or complete, isolated or associated with other malformations. Its prenatal diagnosis creates problems within parental counselling due to its uncertain prognosis. The aim of this study was to correlate the neurodevelopmental outcome with both the clinical picture and the neuroradiological features, in order to improve prenatal parental counselling in a group of nine children with ACC, prenatally diagnosed by ultrasound and then confirmed by postnatal magnetic resonance imaging (MRI).

Methods: In all patients, cerebral ultrasound scans, electroencephalogram (EEG) examinations, cerebral MRI, cytogenetic analysis, general physical evaluation, neurological examination and neuropsychological assessment (Griffiths Scale, Wechsler Primary and Preschool Scale of Intelligence, Wechsler Intelligence Scale for Children) were carried out.

Results: In six patients the callosal agenesis was isolated, while in 3/9 it was associated with other cerebral malformations. Children with isolated callosal agenesis were asymptomatic or presented a mild hypotonia and the EEG was normal in five of them. All children with other associated brain malformations presented epilepsy, poor psychomotor development and cerebral palsy.

Conclusion: The prenatal suspicion of ACC needs an accurate diagnostic approach, in order to well determine its isolated or associated nature, linked to different neurodevelopmental outcome.

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