“…A high incidence of visual perception deficits has been identified in both patients with signs of autism and in those with ID, as also acknowledged by the DSM-5 (APA, 2013). Several studies, mirroring the research in autism, have looked into the frequency of visual deficits in a population of subjects with ID, and found an increased prevalence of visual impairment (Boot et al, 2012;Carvill, 2001), including disturbances in visual orienting behavior, spatial cognition and oculomotor functioning (Boot et al, 2012;Giuliani and Schenk, 2015). Interestingly, Battaglia (2011) underlines that the relationship between sensory deficits and ID is frequent, and that these are also observed in multiple conditions including ASD, the fragile X syndrome, tuberous sclerosis complex associated with ASD, Rett syndrome, 22q13.3 deletion syndrome, familial dysautonomia, Williams syndrome, Down syndrome and Prader-Willi syndrome, but also in other contexts such as a history of neonatal distress, or perinatal brain lesions often accompanying premature birth (Couser et al, 2017;Geldof et al, 2015;Krinsky-McHale et al, 2014).…”