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Updated: May 13, 2026

Eye Tracking Young Children with Autism
Published on: March 27, 2012
White matter microstructure and atypical visual orienting in 7-month-olds at risk for autism
Jed T Elison1, Sarah J Paterson, Jason J Wolff
1Carolina Institute for Developmental Disabilities and Department of Psychiatry, University of North Carolina at Chapel Hill, USA. jelison@caltech.edu
Insights
Infants later diagnosed with autism spectrum disorder (ASD) show delayed visual orienting at 7 months. This atypical visual orienting may be an early sign of ASD, impacting cognitive development.
Area of Science:
- Neurodevelopmental disorders
- Cognitive neuroscience
- Pediatric neurology
Background:
- Autism spectrum disorder (ASD) diagnosis relies on behavioral observation, often later in childhood.
- Early identification of ASD risk factors is crucial for timely intervention.
- Oculomotor functioning and visual orienting are fundamental for cognitive and social development.
Purpose of the Study:
- To investigate if specific oculomotor and visual orienting patterns at 7 months predict later autism spectrum disorder (ASD) diagnosis.
- To identify the neural correlates associated with these early visual behaviors in infants.
Main Methods:
- Eye-tracking and diffusion-weighted imaging were used in a cohort of 97 infants (high-familial-risk and low-risk).
- Infants were assessed at 7 months for visual orienting and brain structure, and clinically at 25 months for ASD diagnosis.
- Saccadic reaction time and radial diffusivity in specific white matter tracts were primary outcome measures.
Main Results:
- Infants later diagnosed with ASD exhibited longer visual orienting latencies at 7 months compared to controls.
- The association between visual orienting and white matter organization (splenium of the corpus callosum) differed between infants who developed ASD and those who did not.
- Abnormal functional specialization in posterior cortical circuits was implicated.
Conclusions:
- Atypical visual orienting in infancy may serve as an early prodromal feature of autism spectrum disorder (ASD).
- These findings suggest a novel model of ASD pathogenesis involving abnormal posterior cortical circuit specialization.
- Efficient visual orienting is vital for subsequent cognitive and social-cognitive development.
Abstract:
OBJECTIVE The authors sought to determine whether specific patterns of oculomotor functioning and visual orienting characterize 7-month-old infants who later meet criteria for an autism spectrum disorder (ASD) and to identify the neural correlates of these behaviors. METHOD Data were collected from 97 infants, of whom 16 were high-familial-risk infants later classified as having an ASD, 40 were high-familial-risk infants who did not later meet ASD criteria (high-risk negative), and 41 were low-risk infants. All infants underwent an eye-tracking task at a mean age of 7 months and a clinical assessment at a mean age of 25 months. Diffusion-weighted imaging data were acquired for 84 of the infants at 7 months. Primary outcome measures included average saccadic reaction time in a visually guided saccade procedure and radial diffusivity (an index of white matter organization) in fiber tracts that included corticospinal pathways and the splenium and genu of the corpus callosum. RESULTS Visual orienting latencies were longer in 7-month-old infants who expressed ASD symptoms at 25 months compared with both high-risk negative infants and low-risk infants. Visual orienting latencies were uniquely associated with the microstructural organization of the splenium of the corpus callosum in low-risk infants, but this association was not apparent in infants later classified as having an ASD. CONCLUSIONS Flexibly and efficiently orienting to salient information in the environment is critical for subsequent cognitive and social-cognitive development. Atypical visual orienting may represent an early prodromal feature of an ASD, and abnormal functional specialization of posterior cortical circuits directly informs a novel model of ASD pathogenesis.
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Autism Spectrum Disorder
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