Abstract
Williams syndrome (WS) and Autism Spectrum Disorders (ASD) are psychiatric conditions associated with atypical but opposite face-to-face interactions patterns: WS patients overly stare at others, ASD individuals escape eye contact. Whether these behaviors result from dissociable visual processes within the occipito-temporal pathways is unknown. Using high-density electroencephalography, multivariate pattern classification and group blind source separation, we searched for face-related neural signals that could best discriminate WS (N = 14), ASD (N = 14) and neurotypical populations (N = 14). We found two peaks in neurotypical participants: the first at 170ms, an early signal known to be implicated in low-level face features, the second at 260ms, a late component implicated in decoding salient face social cues. The late 260ms signal varied as a function of the distance of the eyes in the face stimulus with respect to the viewers’ fovea, meaning that it was strongest when the eyes were projected on the fovea and weakest when projected in the retinal periphery. Remarkably, both components were found distinctly impaired and preserved in WS and ASD. In WS, we could weakly decode the 170ms signal probably due to their relatively poor ability to process faces’ morphology while the late 260ms component shown to be eye sensitive was highly significant. The reverse pattern was observed in ASD participants who showed neurotypical like early 170ms evoked activity but impaired late evoked 260ms signal. Our study reveals a dissociation between WS and ASD patients and point at different neural origins for their social impairments.
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