Seizures during infancy and childhood Flashcards
Types
- Neonatal epilepsy syndrome
- Epilepsy syndromes in children
- Benign focal epilepsies
- Childhood absence
- Juvenile myoclonic
- Infantile spasm
- Neonatal epilepsy syndrome types
Two rare but well-recognized neonatal seizure syndromes are associated with a relatively good prognosis
- Benign (self-limited) neonatal seizures
- Benign familial neonatal epilepsy
Seizures occur within the first seven days of life
Unifocal clonic
- Epilepsy syndromes in children types
The Lennox-Gastaut syndrome is associated with severe seizures in childhood
Genetic syndromes and hypoxic ischemic insults.
Children usually present in the first 7 years of life with a syndrome characterized by multiple seizure types, particularly tonic and atonic seizures, an atypical, slow spike and wave pattern on electroencephalogram (EEG), and mental retardation, often with psychotic features
Benign partial/focal epilepsies of childhood
Idiopathic syndromes that occur in developmentally and neurologically normal children and have a benign course, remitting prior to adulthood
Absence seizures
petit mal or generalized nonconvulsive seizures
The only or most predominant seizure type in several epileptic syndromes, which have markedly different clinical courses and prognoses.
Brief staring episodes with behavioral arrest that may occur tens to hundreds of times daily
Antiepileptic drugs
Phenytoin
Phenobarbital
Ethosuximide
Phenytoin
good for focal and generalized seizures
SE: gingival hypertrophy
Tx: Lennox Gastaut syndrome
Valproic acid, lamotrigine, topiramate
NO carbamazepine
Tx: Benign partial/focal epilepsies of childhood
Antiseizure drug treatment is often not recommended, particularly if only focal seizures without impairment of consciousness occur and if the child and family are comfortable with this approach