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  2. Neonatal seizure - Wikipedia

    en.wikipedia.org/wiki/Neonatal_seizure

    A neonatal seizure is a seizure in a baby younger than age 4-weeks that is identifiable by an electrical ... the goals of management are to identify the cause of the ...

  3. Benign neonatal seizures - Wikipedia

    en.wikipedia.org/wiki/Benign_neonatal_seizures

    Similar to non-familial neonatal seizures, familial seizures may be focal, multifocal clonic, or tonic. The key to diagnosis is a family history of similar events and a normal neurological exam. Seizures occur between a few days to a few weeks of life and resolve by 5 months of age (range 5 days to 2 years).

  4. Benign familial neonatal seizures - Wikipedia

    en.wikipedia.org/wiki/Benign_familial_neonatal...

    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 ]

  5. Benign familial infantile epilepsy - Wikipedia

    en.wikipedia.org/wiki/Benign_familial_infantile...

    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 ...

  6. Benign infantile epilepsy - Wikipedia

    en.wikipedia.org/wiki/Benign_infantile_epilepsy

    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.

  7. Panayiotopoulos syndrome - Wikipedia

    en.wikipedia.org/wiki/Panayiotopoulos_syndrome

    Panayiotopoulos syndrome (named after C. P. Panayiotopoulos) is a common idiopathic childhood-related seizure disorder that occurs exclusively in otherwise normal children (idiopathic epilepsy) and manifests mainly with autonomic epileptic seizures and autonomic status epilepticus. [1]