Significados de epileptiform en inglés

Background: Childhood absence epilepsy is a common generalized epilepsy syndrome characterized by childhood onset of frequent sporadic absence seizures.

We believe that frontal onset absences should be considered as a secondarily generalized epilepsy syndrome, originating in the frontal regions.

All cases reported in 2006-2008 were analyzed retrospectively; available clinical information was reevaluated and classified by seizure type and epilepsy syndrome.

Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is a familial partial epilepsy syndrome characterized by seizures suggesting a frontal lobe origin occurring predominantly during sleep.

Patients with a wide range of epilepsy syndromes and etiologies were registered.

Thus, impairment of potassium-dependent repolarization is likely to cause this age-specific epileptic syndrome.

Generally, West syndrome is an intractable epileptic syndrome in infancy, although spontaneous remission has been reported in some cases.

Treatment is most successful when tailored to the particular seizure type, epileptic syndrome, and special needs of the individual patient.

Lennox-Gastaut syndrome is a severe childhood epileptic syndrome with encephalopathy and multiple seizure types, which are often intractable to treatment.

Generalized epilepsy with febrile seizures plus (GEFS+) is an early onset febrile epileptic syndrome with therapeutic responsive (a)febrile seizures continuing later in life.

Epilepsy is a common seizure disorder affecting approximately 70 million people worldwide.

Sure enough, Seth read that Dustin did have a well-documented seizure disorder.

Edsel had a seizure disorder that required medication and a special diet.

The mother-of-two was diagnosed with PTSD and non-epileptic seizure disorder in 2008.

This area was ultimately resected because of persistence of a severe seizure disorder.