Cognitive functioning in Williams syndrome: a study in Portuguese and Spanish patients

Williams Syndrome (WS) is a genetic neurodevelopmental disorder caused by a submicroscopic deletion on chromosome 7 q11.23. This is a systemic disorder in which cardiac problems and mental retardation are the key phenotypic symptoms. Although displaying a general cognitive impairment, they are most...

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Bibliographic Details
Main Author: Sampaio, Adriana (author)
Other Authors: Férnandez, Montse (author), Henriques, Margarida Rangel (author), Carracedo, Ángel (author), Sousa, Nuno (author), Gonçalves, Óscar F. (author)
Format: article
Language:eng
Published: 2009
Subjects:
Williams Syndrome
Cognitive profile
Neurodevelopment
Science & Technology
Online Access:https://hdl.handle.net/1822/11672
Country:Portugal
Oai:oai:repositorium.sdum.uminho.pt:1822/11672

Internet

https://hdl.handle.net/1822/11672

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