Although overexpression of APP is the most probable cause of AD in individuals with DS, involvement of other genes has also been reported in its pathogenesis (Ermak et al., 2001; Kimura et al., 2007), among which is DSCR1. DSCR1 is highly expressed in the AD brain (Ermak et al., 2001) and is implicated in various types of neuronal stresses linked to AD (Ermak and Davies, 2003; Belmont et al., 2008; Sun et al., 2014). The gene discussed is RCAN1; the disease is Dravet syndrome.