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Neuropsychological Profile of Italian Children and Adolescents with 22q11.2 Deletion Syndrome with and Without Intellectual Disability

✍ Scribed by Stefano Vicari; Manuela Mantovan; Francesca Addona; Floriana Costanzo; Lorena Verucci; Deny Menghini

Book ID
106360988
Publisher
Springer US
Year
2011
Tongue
English
Weight
232 KB
Volume
42
Category
Article
ISSN
0001-8244

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## Abstract 22q11.2 Deletion Syndrome (22q11DS) is the most common genetic microdeletion syndrome affecting humans. The syndrome is associated with general cognitive impairments and specific deficits in visual‐spatial ability, non‐verbal reasoning, and planning skills. 22q11DS is also associated wi

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A microscopic deletion of chromosome 22q11.2 has been identified in most patients with the DiGeorge, velocardiofacial syndrome, conotruncal anomaly face syndrome, and in some patients with isolated conotruncal cardiac anomalies. This study presents the neurodevelopmental outcome, including cognitive