Dravet syndrome is a rare, catastrophic, lifelong form of epilepsy that begins in the first year of life with frequent and/or prolonged seizures. Previously ...

Certain seizure disorders such as Lennox-Gastaut syndrome (LGS), Dravet syndrome, and tuberous sclerosis complex (TSC) are not always easy to diagnose.

Relatively rare causes of adult onset seizure were acute disseminated encephalomyelitis (ADEM), multiple sclerosis (MS), and posterior reversible ...

Progressive myoclonic epilepsy is rare and frequently results from hereditary metabolic disorders, such as neuronal ceroid lipofuscinosis and mitochondrial ...

Seizure disorders commonly begin in early childhood or in late adulthood. ... Epilepsia partialis continua is rare. In this type of seizure, focal seizures ...

Structural epilepsies · Angiocentric Glioma (ANET) · Arteriovenous malformation · Astrocytoma Variants · Cerebellar hamartoma · Cerebral Angioma with epilepsy

We will provide general, high-level information for a select group of epilepsy syndromes, such as West Syndrome, Dravet syndrome, and Lennox-Gastaut syndrome.

Benign adult familial myoclonic epilepsy (BAFME) is an inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional ...

3 сент. 2013 г. · An epilepsy syndrome is a type of epilepsy that is identified by a specific seizure type or types and by the findings on an EEG. Myoclonic Epilepsy in Infancy · Early Infantile Developmental...

In reflex epilepsy, a rare disorder, seizures are triggered predictably by an external stimulus, such as repetitive sounds, flashing lights, video games, music, ...