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A cross-syndrome study of the development of holistic face recognition in children with autism, Down syndrome, and Williams syndrome.

Abstract
We report a cross-syndrome comparison of the development of holistic processing in face recognition in school-aged children with developmental disorders: autism, Down syndrome, and Williams syndrome. The autism group was split into two groups: one with high-functioning children and one with low-functioning children. The latter group has rarely been studied in this context. The four disorder groups were compared with typically developing children. Cross-sectional trajectory analyses were used to compare development in a modified version of Tanaka and Farah's part-whole task. Trajectories were constructed linking part-whole performance either to chronological age or to several measures of mental age (receptive vocabulary, visuospatial construction, and the Benton Facial Recognition Test). In addition to variable delays in onset and rate of development, we found an atypical profile in all disorder groups. These profiles were atypical in different ways, indicating multiple pathways to, and variable outcomes in, the development of face recognition. We discuss the implications for theories of face recognition in both atypical and typical development, including the idea that part-whole and rotation manipulations may tap different aspects of holistic and/or configural processing.
AuthorsDagmara Annaz, Annette Karmiloff-Smith, Mark H Johnson, Michael S C Thomas
JournalJournal of experimental child psychology (J Exp Child Psychol) Vol. 102 Issue 4 Pg. 456-86 (Apr 2009) ISSN: 1096-0457 [Electronic] United States
PMID19193384 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Autistic Disorder (epidemiology)
  • Child
  • Child, Preschool
  • Cognition Disorders (diagnosis, epidemiology)
  • Down Syndrome (epidemiology)
  • Face
  • Facial Expression
  • Female
  • Humans
  • Male
  • Neuropsychological Tests
  • Recognition, Psychology
  • Visual Perception
  • Williams Syndrome (epidemiology)

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