Synonyms:
a.k.a. Dravet’s syndrome
Genetics:
Na+ SCN1A 2q24 de novo mutations
Clinical features:
Onset <1y.o., tonic-clonic seizures
Later; myclonic, absense & partial seizures
+speech & motor arrest & reduced life expectancy
Treatment:
Valproate VPA
Topiramate TPM, clonazepam, clobazam