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Epilepsia - BLF

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B<br />

F<br />

N<br />

S<br />

O<br />

S<br />

Benign<br />

familial<br />

infantile<br />

seizures<br />

Migrating<br />

focal<br />

seizures<br />

of early<br />

infancy<br />

Benign nonfamilial infantile<br />

seizures<br />

West<br />

syndrome<br />

Benign myoclonic epilepsy of infancy<br />

Hemiconvulsion-hemiplegia syndrome<br />

Rasmussen syndrome<br />

Myoclonic astatic<br />

epilepsy<br />

Continuous SW during Slow Sleep - CSWSS<br />

Landau Kleffner<br />

syndrome<br />

Benign childhood epilepsy with centrotemporal<br />

spikes<br />

Early onset benign childhood occipital epilepsy – Panayiotopoulos type<br />

Startle epilepsy<br />

Epilepsy syndromes<br />

Late onset benign childhood occipital epilepsy- Gastaut type<br />

Generalized epilepsies with febrile seizures plus<br />

Autosomal dominant frontal lobe epilepsy<br />

Juvenile absence<br />

Childhood absence epilepsy epilepsy<br />

Epilepsy with myoclonic absences<br />

Visual sensitive epilepsies<br />

Progressive myoclonus epilepsies<br />

/<br />

Myoclonic status in nonprogressive encephalopathies<br />

E<br />

M<br />

Lennox-Gastaut<br />

E Dravet syndrome<br />

syndrome<br />

Reading<br />

epilepsy<br />

Familial lateral temporal lobe epilepsy<br />

Epilepsy with generalized tonic-clonic<br />

seizures only<br />

Juvenile myoclonic epilepsy<br />

Idiopathic<br />

photosensitive<br />

occipital lobe<br />

epilepsy<br />

½ 1<br />

2 5 10 15 20 years<br />

Age at<br />

onset

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