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   <subfield code="a">Brief Report: Visual-Spatial Deficit in a 16-year-old Girl with Maternally Derived Duplication of Proximal 15q</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[David Cohen, Claire Martel, Anna Wilson, Nicole Déchambre, Céline Amy, Ludovic Duverger, Jean-Marc Guile, Eva Pipiras, Brigitte Benzacken, Hélène Cavé, Laurent Cohen, Delphine Héron, Monique Plaza]</subfield>
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   <subfield code="a">Duplications of chromosome 15 may be one of the most common single genetic causes of autism spectrum disorders (ASD), aside from fragile X. Most of the cases are associated with maternally derived interstitial duplication involving 15q11-13. This case report describes a female proband with a maternally derived interstitial duplication of proximal 15q. She did not exhibit any symptoms of ASD apart from some developmental delay. By adolescence, she showed mild dysmorphism, a discrepant profile on the Wechsler Intelligence Scale for Children (Verbal IQ=87; Performance IQ=65) and a major deficit in visual-spatial abilities affecting fine motor skills, mathematical reasoning, visual memory and some global reading tasks. This is one of the first reports of a child with a maternal duplication who exhibits a visual-spatial deficit without ASD.</subfield>
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   <subfield code="a">Chromosome 15</subfield>
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   <subfield code="a">Prader-Willi/Angelman Syndrome critical region</subfield>
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   <subfield code="a">Maternally derived interstitial duplication</subfield>
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   <subfield code="a">Pervasive developmental disorder</subfield>
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   <subfield code="u">CNRS, &quot;Cognition et comportement”, Université Paris V, Boulogne, France</subfield>
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   <subfield code="t">Journal of Autism and Developmental Disorders</subfield>
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