Learning to read in Williams syndrome and Down syndrome: syndrome-specific precursors and developmental trajectories

2013 ◽  
Vol 54 (7) ◽  
pp. 754-762 ◽  
Author(s):  
Ann Steele ◽  
Gaia Scerif ◽  
Kim Cornish ◽  
Annette Karmiloff-Smith
2012 ◽  
Vol 40 (1) ◽  
pp. 106-138 ◽  
Author(s):  
YONATA LEVY ◽  
ARIELA EILAM

ABSTRACTThis is a naturalistic study of the development of language in Hebrew-speaking children with Williams syndrome (WS) and children with Down syndrome (DS), whose MLU extended from 1·0 to 4·4. Developmental curves over the entire span of data collection revealed minor differences between children with WS, children with DS, and typically developing (TD) controls of similar MLU. Development within one calendar year showed remarkable synchrony among the variables. However, age of language onset and pace of acquisition departed significantly from normal timing. It is argued that in view of the centrality of genetic timing and the network properties of cognition, normal schedules are crucial determinants of intact development. Consequently, with respect to neurodevelopmental syndromes, the so-called ‘language delay’ is indicative of deviance that is likely to impact development in critical ways.


2016 ◽  
Vol 55 ◽  
pp. 64-76 ◽  
Author(s):  
Henrik Danielsson ◽  
Lucy Henry ◽  
David Messer ◽  
Daniel P.J. Carney ◽  
Jerker Rönnberg

2003 ◽  
Vol 41 (8) ◽  
pp. 1037-1046 ◽  
Author(s):  
Janice H Brown ◽  
Mark H Johnson ◽  
Sarah J Paterson ◽  
Rick Gilmore ◽  
Elena Longhi ◽  
...  

2020 ◽  
Vol 50 (12) ◽  
pp. 4553-4556 ◽  
Author(s):  
Hannah Harvey ◽  
Maria Ashworth ◽  
Olympia Palikara ◽  
Jo Van Herwegen

2020 ◽  
Vol 33 (5) ◽  
pp. 1080-1089 ◽  
Author(s):  
Jo Van Herwegen ◽  
Erica Ranzato ◽  
Annette Karmiloff‐Smith ◽  
Victoria Simms

2015 ◽  
Vol 59 (1) ◽  
pp. 25487 ◽  
Author(s):  
Marianne Nordstrøm ◽  
Benedicte Paus ◽  
Lene F. Andersen ◽  
Svein Olav Kolset

2016 ◽  
Vol 29 (4) ◽  
pp. 1189-1197 ◽  
Author(s):  
Karen J. Goldman ◽  
Cory Shulman ◽  
Yair Bar-Haim ◽  
Rany Abend ◽  
Jacob A. Burack

AbstractIndividuals with Williams syndrome and those with Down syndrome are both characterized by heightened social interest, although the manifestation is not always similar. Using a dot-probe task, we examined one possible source of difference: allocation of attention to facial expressions of emotion. Thirteen individuals with Williams syndrome (mean age = 19.2 years, range = 10–28.6), 20 with Down syndrome (mean age = 18.8 years, range = 12.1–26.3), and 19 typically developing children participated. The groups were matched for mental age (mean = 5.8 years). None of the groups displayed a bias to angry faces. The participants with Williams syndrome showed a selective bias toward happy faces, whereas the participants with Down syndrome behaved similarly to the typically developing participants with no such bias. Homogeneity in the direction of bias was markedly highest in the Williams syndrome group whose bias appeared to result from enhanced attention capture. They appeared to rapidly and selectively allocate attention toward positive facial expressions. The complexity of social approach behavior and the need to explore other aspects of cognition that may be implicated in this behavior in both syndromes is discussed.


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