“…Slon, Hershkovitz, and Peled () reported a case of a historical patient that is a 6,000‐year‐old skeleton of an adult male with DDMS. Classically, patients present a varying extent of facial asymmetry or paresis, sensory disturbances, hemiatrophy of body, focal or generalized uncontrolled seizures, contralateral hemiplegia, mental retardation, impaired cognition, learning and speech impairment, and psychiatric problems (Behera, Patnaik, & Mohanty, ; Shrestha, ; Tasdemir, Incesu, Yazicioglu, Belet, & Güngör, ). The syndrome may be either congenital or acquired (e.g., following trauma, infection, or a vascular disorder; Atalar, Icagasioglu, & Tas, ).…”