Dravet syndrome is a rare and severe type of epilepsy. "Severe myoclonic epilepsy in infancy" was first described in 1978 by Charlotte Dravet, who observed common features: onset in the first year of...

Our knowledge on epileptic spasms and West syndrome is always in progress. Its wide variability concerning clinical semiology, EEG patterns and neurodevelopment is related to heterogeneous aetiologies...

Epilepsy and migraine are two frequent chronic neurological disorders which have complex links. Their comorbidity is well established by epidemiological data. Both are characterized by recurrent epileptic...

Since 1984, the year of the publication of its first edition, the famous “Blue Guide” has been the international reference for paediatricians and neuropaediatricians with regard to epileptic syndromes...