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Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations
by
Menghetti, Sarah
, Zaharia, Alexandra
, Debbané, Martin
, Eliez, Stephan
, Schaer, Marie
, Schneider, Maude
, Glaser, Bronwyn
, Franchini, Martina
in
Accuracy
/ Adolescents
/ Autism
/ Bias
/ Biomedical and Life Sciences
/ Biomedicine
/ Children
/ Children & youth
/ Configural face processing
/ Data processing
/ Emotions
/ Eye-tracking
/ Face
/ Featural face processing
/ Genotype & phenotype
/ Human Genetics
/ Neurodevelopmental disorders
/ Neurology
/ Neuropsychology
/ Neurosciences
/ NMR
/ Nuclear magnetic resonance
/ Pattern recognition
/ Pediatrics
/ Psychiatry
/ Social difficulties
/ Social interactions
/ Studies
/ Teenagers
/ Visual discrimination
2018
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Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations
by
Menghetti, Sarah
, Zaharia, Alexandra
, Debbané, Martin
, Eliez, Stephan
, Schaer, Marie
, Schneider, Maude
, Glaser, Bronwyn
, Franchini, Martina
in
Accuracy
/ Adolescents
/ Autism
/ Bias
/ Biomedical and Life Sciences
/ Biomedicine
/ Children
/ Children & youth
/ Configural face processing
/ Data processing
/ Emotions
/ Eye-tracking
/ Face
/ Featural face processing
/ Genotype & phenotype
/ Human Genetics
/ Neurodevelopmental disorders
/ Neurology
/ Neuropsychology
/ Neurosciences
/ NMR
/ Nuclear magnetic resonance
/ Pattern recognition
/ Pediatrics
/ Psychiatry
/ Social difficulties
/ Social interactions
/ Studies
/ Teenagers
/ Visual discrimination
2018
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Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations
by
Menghetti, Sarah
, Zaharia, Alexandra
, Debbané, Martin
, Eliez, Stephan
, Schaer, Marie
, Schneider, Maude
, Glaser, Bronwyn
, Franchini, Martina
in
Accuracy
/ Adolescents
/ Autism
/ Bias
/ Biomedical and Life Sciences
/ Biomedicine
/ Children
/ Children & youth
/ Configural face processing
/ Data processing
/ Emotions
/ Eye-tracking
/ Face
/ Featural face processing
/ Genotype & phenotype
/ Human Genetics
/ Neurodevelopmental disorders
/ Neurology
/ Neuropsychology
/ Neurosciences
/ NMR
/ Nuclear magnetic resonance
/ Pattern recognition
/ Pediatrics
/ Psychiatry
/ Social difficulties
/ Social interactions
/ Studies
/ Teenagers
/ Visual discrimination
2018
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Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations
Journal Article
Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations
2018
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Overview
Background
Previous research links social difficulties to atypical face exploration in 22q11.2 deletion syndrome (22q11.2DS). Two types of face processing are distinguished: configural (CFP) and featural (FFP). CFP develops later in life and plays an important role in face and emotion recognition abilities. Recent studies reported atypical development of CFP in several neurodevelopmental disorders. Taking previous reports of atypical face exploration one step further, our study aims at characterizing face processing in children and adolescents with 22q11.2DS. First, we sought to identify biases in the first two fixation positions on faces and to detect differences between CFP and FFP in 22q11.2DS using eye-tracking technology. Second, we investigated the developmental trajectories of CFP and FFP using accuracy data from follow-up evaluation.
Methods
Seventy-five individuals with 22q11.2DS and 84 typically developed (TD) individuals (aged 6–21 years) completed a discrimination task (“Jane task”) inducing CFP and FFP in an eye-tracking setting. Thirty-six individuals with 22q11DS and 30 TD from our sample completed a longitudinal follow-up evaluation.
Results
Findings revealed that individuals with 22q11.2DS demonstrate an early bias toward the mouth region during the initial fixations on the faces and reduced flexibility exploration of the faces, with a reduced number of transitions between faces and longer fixations compared to the TD group. Further, scanpaths did not differ between CFP and FFP in the 22q11.2DS group. Longitudinal analysis of accuracy data provided evidence for atypical development of CFP in 22q11.2DS.
Conclusions
The current study brings new evidence of altered face exploration in 22q11.2DS and identifies developmental mechanisms that may contribute to difficulties impacting social interactions in the syndrome.
Publisher
BioMed Central,Springer Nature B.V,BMC
Subject
/ Autism
/ Bias
/ Biomedical and Life Sciences
/ Children
/ Emotions
/ Face
/ Neurodevelopmental disorders
/ NMR
/ Studies
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