SCN1A and movement disorder: Recently, novel SCN1A-related phenotypes have been described, including severe DEEs of non-Dravet syndromes: neonatal developmental and epileptic encephalopathy with a movement disorder and arthrogryposis (NDEEMA), developmental and epileptic encephalopathy with a movement disorder (EIDEE/MD), epileptic encephalopathy (EIDEE) [15].