“…Moreover, humans affected by either congenital or acquired conditions where portions of the brain are severely underdeveloped or missing can have normal or near-normal intelligence and cognitive skills, with examples including some severe forms of microcephaly (Haslam and Smith, 1979; Kozma et al, 1996); childhood hemispherectomy (i.e., disconnection or removal of an entire cerebral hemisphere; Borgstein and Grootendorst, 2002; Devlin et al, 2003; Liégeois et al, 2010; Pulsifer et al, 2004); a patient born with only one hemisphere (Muckli et al, 2009); craniopagus malformation (Lansdell, 1999; Stone and Goodrich, 2006; Todorov et al, 1974), including a pair of craniopagus twins that share a brain and mind (Squair, 2012); individuals with almost complete absence of the cerebellum (Glickstein, 1994; Yu et al, 2015); and a case of severe hydrocephaly (Feuillet et al, 2007). Nevertheless, how a simple change in brain size or neuron and/or glia number could lead to differences in cognitive capabilities is not, at a mechanistic level, well understood.…”