Einführung: Frühkindliche Epilepsien und epileptische Syndrome
摘要
Epilepsy often begins early in life and can place a considerable burden on affected children and their families.
ObjectiveDescription of the epilepsy syndromes that typically begin in the first 2 years of life.
Material and methodsThe focus is on the classification and definition of epilepsy syndromes.
ResultsEpilepsy syndromes that begin in the first 2 years of life are generally divided into 2 large groups: Self-limited epilepsies with a high likelihood of spontaneous remission and a good prognosis, and developmental and epileptic encephalopathies. In the latter case, developmental disorders occur both because of the underlying etiology —regardless of epileptic activity— and as a result of seizure activity. Most syndromes with a specific etiology in newborns and infants also belong to the developmental and epileptic encephalopathies.
ConclusionKnowledge of the classification of epilepsies with onset in the first 2 years of life enables individualized counselling and treatment and helps to better meet the needs of young children with epilepsy and their families.