Previously reported patients with DNM1‐related disorder carry pathogenic variants in the GTPase or middle domains, but never in the PH domain (Allen et al., 2016; Deng et al., 2016; Epi4K Consortium; Epilepsy Phenome/Genome Project, 2013; Euro E‐RESC, EpilepsyPhenome/Genome P, Epi4K Constorium, 2014; Nakashima et al., 2016). This evidence concerns the gene DNM1 and epilepsy.