“…In fact, congenital agenesis of the CC permits developmental adaptive reorganizations (Paul, 2011;Paul et al, 2007); therefore, it is not surprising that individuals without a CC from birth frequently exhibit less severe symptoms of disconnection syndrome compared with patients that underwent surgical transection of the CC during life (Brown et al, 2001;Chiarello, 1980;. In spite of this, however, reports of these cases produce a picture characterized by inconsistencies, as they describe clear examples of FC asymmetries as well as no sign of functional disruption in patients with congenital agenesis (Paul and Tyszka, 2012).…”