Cognitive impairment in children with CACNA1A mutations.
Veronique HumbertclaudeFlorence RiantBenjamin KramsValerie ZimmermannNicolas NagotDaniel AnnequinBernard EchenneElisabeth Tournier-LasserveAgathe Roubertienull nullPublished in: Developmental medicine and child neurology (2019)
Cognitive disabilities and academic difficulties are common in children with CACNA1A mutations associated with episodic syndromes. Cognitive function ranges from normal to moderate intellectual disorder in wheelchair-dependent children. Patients with vermian atrophy are at a higher risk of cognitive impairment.