| Literature DB >> 17006777 |
David Cohen1, 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.
Abstract
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.Entities:
Mesh:
Year: 2006 PMID: 17006777 DOI: 10.1007/s10803-006-0228-5
Source DB: PubMed Journal: J Autism Dev Disord ISSN: 0162-3257