Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum. (January 2017)

• Record Type: Journal Article
• Authors: Romaniello, Romina; Marelli, Susan; Giorda, Roberto; Bedeschi, Maria F.; Bonaglia, Maria C.; Arrigoni, Filippo; Triulzi, Fabio; Bassi, Maria T.; Borgatti, Renato
• Is Part Of: Journal of child neurology. Volume 32:Number 1(2017:Jan.)
• Page Start: 60
• Page End: 71
• Publication Date: 2017-01
• Subjects: corpus callosum -- brain malformations -- intellectual disability -- genetic -- array-CGH; Nervous system -- Diseases -- Periodicals; 618.928
• DOI: 10.1177/0883073816664668
• Languages: English
• ISSNs: 0883-0738

Abstract

To gain a better understanding of the clinical and genetic features associated with agenesis of corpus callosum, we enrolled and characterized 162 patients with complete or partial agenesis of corpus callosum. Clinical and genetic protocols allowed us to categorize patients as syndromic subjects, affected by complex extra-brain malformations, and nonsyndromic subjects without any additional anomalies. We observed slight differences in sex ratio (56% males) and agenesis type (52% complete). Syndromic agenesis of corpus callosum subjects were prevalent (69%). We detected associated cerebral malformations in 48% of patients. Neuromotor impairment, cognitive and language disorders, and epilepsy were frequently present, regardless of the agenesis of corpus callosum subtype. Long-term follow-up allowed us to define additional indicators: syndromic agenesis of corpus callosum plus patients showed the most severe clinical features while isolated complete agenesis of corpus callosum patients had the mildest symptoms, although we observed intellectual disability (64%) and epilepsy (15%) in both categories. We achieved a definitive (clinical and/or genetic) diagnosis in 42% of subjects.