For Ohtahara syndrome (early infantile epileptic encephalopathy [EIEE]), a number of different genetic causes have been found in recent years, including genes for a neuronal voltage-sensitive potassium channel (KCNQ2), a sodium channel of excitatory neurons (SCN2A), and a synaptic protein involved in the exocytosis of neurotransmitters (STXBP1), among numerous other rare genes [7]. Here, SCN2A is linked to early-infantile DEE.