Epilepsy phenotype in patients with Xp22.31 microduplication

We describe a family in which mother and two children have Xp22.31 microduplication associated with different forms of epilepsy and epileptiform EEG abnormalities. The proband had benign epilepsy with centrotemporal spikes with dysgraphia and dyscalculia (IQ 72), the sister had juvenile myoclonic epilepsy, and both had bilateral talipes anomalies. The mother, carrier of the microduplication, was asymptomatic. The asymptomatic father did not present microduplication. These data contribute to delineate the phenotype associated with Xp22.31 microduplication and suggest its pathogenic role, probably additive, also for the epilepsy phenotype.

Source: Epilepsy and Behavior Case Reports - November 6, 2018 Category: Neurology Source Type: research