Abstract
One might expect that children with varying genetic mutations or children raised in low socioeconomic status environments would display different deficits. Although this expectation may hold for phenotypic outcomes in older children and adults, cross-syndrome comparisons in infancy reveal many common neural and sociocognitive deficits. The challenge is to track dynamic trajectories over developmental time rather than focus on end states like in adult neuropsychological studies. We contrast the developmental and adult approaches with examples from the cognitive and social domains, and we conclude that static models of adult brain lesions cannot be used to account for the dynamics of change in genetic and environmentally induced disorders in children.
| Original language | English |
|---|---|
| Pages (from-to) | 17261-17265 |
| Journal | Addiction |
| Volume | 109 |
| Issue number | Sup. 2 |
| DOIs | |
| Publication status | Published - 16 Oct 2012 |
Bibliographical note
Note: This work was supported by the Medical Research Council [grant number G0800554] and the Economicand Social Research Council.
Keywords
- autism
- down syndrome
- infant development
- number development
- social cognition
- Williams syndrome
- Biological sciences