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Visuospatial and Numerical Cognitive Deficits in Children with Chromosome 22Q11.2 Deletion Syndrome

✍ Scribed by Tony J. Simon; Carrie E. Bearden; Donna McDonald Mc-Ginn; Elaine Zackai


Book ID
117088521
Publisher
Masson, Italy (now Elsevier Masson)
Year
2005
Tongue
English
Weight
163 KB
Volume
41
Category
Article
ISSN
0010-9452

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## Abstract The 22q11 chromosomal deletion syndrome (22q11DS) is associated with a heterogeneous physical phenotype, neurocognitive deficits, and increased risk of later psychiatric illness. Sporadic clinical reports suggested motor differences, but quantitative studies of movement in children with

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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