The rates of epilepsy among children with autism spectrum disorders (ASD) are higher than that of the general population. The exact prevalence and aetiology of the comorbidity of autism and epilepsy are not well understood; however, the connection is well-documented. This common comorbidity makes the treatment of epilepsy increasingly complex for…

Children with developmental disabilities are at increased risk for epilepsy with a prevalence rate higher than the general population. Some of the more common developmental disorders in childhood and the features of epilepsy in these conditions are discussed. Specifically, autism, cerebral palsy, mental retardation, and attention deficit and…

This commentary reviews studies of children with Landau-Kleffner Syndrome (LKS) and autistic regression (AR) and concludes that they are two distinct entities with different epileptic profiles and that the treatment modalities used in LKS cannot be expected to yield a therapeutic effect in AR. Multiple Subpial Transection is discussed. (Contains…

The treatment of seizure disorders and EEG epileptiform abnormalities without epilepsy in children with autism spectrum disorders in considered within the context of the relationship epilepsy and epileptiform disorders to language, behavior, and cognition. The use of anticonvulsants to treat epileptiform discharges thought to be producing…

Epileptic encephalopathies are progressive clinical and electroencephalographic syndromes where deterioration is thought to be caused by frequent seizures and abundant EEG epileptiform activity. Seizures occur in approximately 10-15% of children with pervasive developmental disorders (PDD) and 8-10% have epileptiform EEG abnormalities without…