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The aim of this single‐centre case series was to describe the long‐term outcomes of children with prenatally diagnosed isolated complete corpus callosum agenesis (cACC). Three infants (11.5%) had a severe neurodevelopmental impairment, two of which with a genetic condition recognised after birth. In 88% of the children with cACC included in our study, neurodevelopment was not severely impaired.
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