Mutations in KCNT1 gene have been found in different epilepsy syndromes: ADNFLE (Heron et al., 2012; Kim et al., 2014; Møller et al., 2015), epilepsy of infancy with migrating focal seizures (EIMFS, previously known as malignant migrating partial seizures in infancy, MMPSI or also more recently as malignant migrating focal seizures of infancy, MMFSI) (Barcia et al., 2012; Ishii et al., 2013; Ohba et al., 2015; Rizzo et al., 2016) and other types of EOEEs, (Vanderver et al., 2014; Ohba et al., 2015), including Ohtahara syndrome (OS) (Martin et al., 2014). Here, KCNT1 is linked to autosomal dominant nocturnal frontal lobe epilepsy.