The International Classification of Epilepsies and Epilepsy Syndromes divides epilepsy, first, on the basis of whether the seizures are partial (localization-related epilepsies) or generalized; and, second, by etiology (idiopathic, symptomatic, or cryptogenic). (The idiopathic partial seizures are discussed in Chapter 16). Symptomatic epilepsies comprise syndromes based on anatomical localization and are considered to be the consequence of a known or suspected disorder of the central nervous system. Cryptogenic epilepsies are presumed to be symptomatic, but the etiology is not clear.
EtiologyBy definition, partial seizures imply the presence of a focal abnormality in one cerebral hemisphere. A definite etiological factor can often be identified by magnetic resonance imaging (MRI). These factors include birth asphyxia, intrauterine infections, congenital brain structural abnormalities, head trauma, meningitis, viral encephalitis, parasitic infections, neoplasms, arteriovenous malformations, stroke, and neurocutaneous diseases (e.g., tuberous sclerosis complex, hypomelanosis of Ito, neurofibromatosis).Epilepsy in Children and Adolescents, First Edition. Edited by James W. Wheless.