Self-limited familial neonatal epilepsy

A neonatal/infantile epilepsy syndrome that is characterized by the onset of seizures that start in the in the neonate between day 1 and 7 of life and are often unilateral clonic events that recur and may alternate sides from seizure to seizure. Seizures can be repetitive over hours to days. Seizures remit by 4-6 months of age. A proportion of those affected may have seizures in later life. The child is expected to have typical developmental progress.

Also known as: self-limited familial and non-familial neonatal seizures, self-limited familial neonatal-infantile epilepsy

7 clinical trials for this condition and its sub-types, 0 tagged with Self-limited familial neonatal epilepsy itself.