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Benign infantile epilepsy (BIE), also known as benign infantile seizures (BIS), is an epilepsy syndrome of which several forms have been described. The International League Against Epilepsy (ILAE) classify two main forms of the syndrome (familial and nonfamilial) [1] though several other forms have been described in the academic literature.
Benign familial infantile epilepsy (BFIE) is an epilepsy syndrome. [1] Affected children, who have no other health or developmental problems, develop seizures during infancy. These seizures have focal origin within the brain but may then spread to become generalised seizures. The seizures may occur several times a day, often grouped in clusters ...
Benign familial neonatal seizures (BFNS), also referred to as benign familial neonatal epilepsy (BFNE), is a rare autosomal dominant inherited form of seizures. This condition manifests in newborns as brief and frequent episodes of tonic-clonic seizures with asymptomatic periods in between. [ 2 ]
i. Self-limited epilepsy with centrotemporal spikes (SeLECTS) SeLECTS, (previously known as benign epilepsy of childhood with centrotemporal spikes or benign Rolandic epilepsy) is a focal epilepsy of unknown cause that most commonly occurs in early to mid school-aged children. Apart from their seizure disorder, these patients are otherwise normal.
Benign Rolandic epilepsy or self-limited epilepsy with centrotemporal spikes (formerly benign childhood epilepsy with centrotemporal spikes (BECTS)) is the most common epilepsy syndrome in childhood. [ 1 ] [ 2 ] Most children will outgrow the syndrome (it starts around the age of 3–13 with a peak around 8–9 years and stops around age 14 ...
Benign neonatal seizures include two disorders: self-limited (benign) ... diagnosis should include no family history of neonatal seizures or epilepsy, appropriate ...