Prenatal diagnosis of agenesis of corpus callosum: what is the neurodevelopmental outcome?
Article first published online: 24 MAY 2006
Volume 48, Issue 3, pages 298–304, June 2006
How to Cite
FRANCESCO, P., MARIA-EDGARDA, B., GIOVANNI, P., DANDOLO, G. and GIULIO, B. (2006), Prenatal diagnosis of agenesis of corpus callosum: what is the neurodevelopmental outcome?. Pediatrics International, 48: 298–304. doi: 10.1111/j.1442-200X.2006.02208.x
- Issue published online: 24 MAY 2006
- Article first published online: 24 MAY 2006
- Received 24 November 2004; revised 19 April 2005; accepted 4 July 2005.
- brain malformation;
- corpus callosum;
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.