Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.
(Sadleir L, et. al 2017). Dravet syndrome is often thought to be at the severe end of a spectrum of SCN1A disorders ranging from relatively mild conditions such as migraines to generalized epilepsy with febrile seizures plus (GEFS+) to DS. Even within the “severe” category of DS, patients can present with a wide degree of […]
