What is Childhood Absence Epilepsy?
Absence seizures are generalized seizures that occur in school-aged children usually between the ages of 5 and 9. Sometimes CAE can be inherited, but it can also occur as a sporadic event. Typical absence seizures consist of sudden cessation of movement, staring, and sometimes blinking. Sometimes, there may be a mild loss of body tone, causing the child to lean forwards or backwards slightly. Unlike other types of seizures, absence seizures occur without an aura or warning. When diagnosing CAE, typical absence seizures need to be differentiated from atypical absence seizures which can occur at an earlier age. An EEG of a child with CAE will show a typical pattern known as 3-Hz generalized spike and wave complexes.
Many children with CAE have normal neurological examinations and intellectual abilities. However, some children may have developmental and intellectual impairments and may have other types of seizures including, but not limited to, tonic clonic seizures.
How is Childhood Absence Epilepsy Treated?
The medications that are usually used to treat CAE include ethosuximide and valproic acid, but other medications can also be used successfully. Usually children are treated for a minimum of 2 years.
What is the prognosis?
The prognosis for CAE is excellent. Remission can be achieved in approximately 80% of patients. Close attention must be paid to seizure control to avoid and academic or social difficulties.