DNM1L and Encephalopathy: Whole-exome sequencing revealed a heterozygous <i>de novo</i> variant in the GTPase domain of <i>DNM1L</i> [NM_001278464.1: c.176C>A p.(Thr59Asn)] making her the oldest patient suffering from encephalopathy due to defective mitochondrial and peroxisomal fission-1.