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SEIZURES

10% prevalence.
Febrile seizures- 3% of the population

Generalized-
- Tonic / clonic / tonic-clonic
- Absence
- Infantile spasms
o Primary
o Secondary
 Landau-Kleffner- verbal skills loss, generalized seizures, poor prognosis.
Tx- everything (anti-epileptic, BZD, steroids, IVIg..)
- Myoclonic-
o Benign of infancy- 2y>. No Tx, good prognosis.
o Of early childgood- 2y<, moderate prognosis
o Juvenile- 12y<, (the hair combers), Tx with valproic acid for life.
o Complex- Lennox-Gastaut- accompanying HIE, combined with
tonic-clonic seizures, poor prognosis.
o Progressive- associated with mitochondrial / metabolic diseases.

Partial seizures-
- Simple- no loss of consciousness (motor, sensory, autonomic..)
- Complex- with loss of consciousness
- Partial seizures with generalization
 Rolandic- centro-temporal region, usually falling asleep or waking up.
 Rasmussen encephalitis- ~10y, ongoing partial seizure, associated with
hemiplegia, poor prognosis

Treatments-
- Effective for all- carbamazepine, valproic acid, Phenobarbital, phenytoin
- Myoclonic- valproic acid
- Hypsarrythmia- steroids (ACTH), vigabatrin (sabril)
- Adjuvants- clobazam (frisium), gabapentin (neurontin), topiramate
(topamax), lamotrigine (lamictal)
 Ethosuximide- for absence (worsening generalized seizures)

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