Literature DB >> 18950649

Dorsal and ventral stream mediated visual processing in genetic subtypes of Prader-Willi syndrome.

Kate A Woodcock1, Glyn W Humphreys, Chris Oliver.   

Abstract

Previous work has suggested that there are specific deficits in dorsal stream processing in a variety of developmental disorders. Prader-Willi syndrome (PWS) is associated with two main genetic subtypes, deletion and disomy. Relative strengths in visual processing are shown in PWS, although these strengths may be specific to the deletion subtype. We investigated visual processing in PWS using an adapted Simon task which contrasted location (dorsal stream) and shape identity (ventral stream) tasks. Compared to a group of typically developing children, children with PWS deletion showed a greater degree of impairment in the dorsal stream task than in the ventral stream task, a pattern similar to that shown in a group of boys with Fragile-X syndrome. When matched on a measure of non-verbal ability, children with PWS disomy showed the opposite pattern with better performance in the location compared to the shape task, although these task performance asymmetries may have been linked to executive control processes. It is proposed that children with PWS deletion show a relative strength in visual processing in the ventral stream along with a specific deficit in dorsal stream processing. In contrast, children with PWS disomy show neither effect.

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Year:  2008        PMID: 18950649     DOI: 10.1016/j.neuropsychologia.2008.09.019

Source DB:  PubMed          Journal:  Neuropsychologia        ISSN: 0028-3932            Impact factor:   3.139


  5 in total

1.  The neuroanatomy of genetic subtype differences in Prader-Willi syndrome.

Authors:  Robyn A Honea; Laura M Holsen; Rebecca J Lepping; Rodrigo Perea; Merlin G Butler; William M Brooks; Cary R Savage
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2012-03       Impact factor: 3.568

2.  Clinical management of behavioral characteristics of Prader-Willi syndrome.

Authors:  Alan Y Ho; Anastasia Dimitropoulos
Journal:  Neuropsychiatr Dis Treat       Date:  2010-05-06       Impact factor: 2.570

3.  Incidental memory for faces in children with different genetic subtypes of Prader-Willi syndrome.

Authors:  Alexandra P Key; Elisabeth M Dykens
Journal:  Soc Cogn Affect Neurosci       Date:  2017-06-01       Impact factor: 3.436

4.  Learning by observation and learning by doing in Prader-Willi syndrome.

Authors:  Francesca Foti; Deny Menghini; Enzo Orlandi; Cristina Rufini; Antonino Crinò; Sabrina Spera; Stefano Vicari; Laura Petrosini; Laura Mandolesi
Journal:  J Neurodev Disord       Date:  2015-02-26       Impact factor: 4.025

5.  Low vision due to cerebral visual impairment: differentiating between acquired and genetic causes.

Authors:  Daniëlle G M Bosch; F Nienke Boonstra; Michèl A A P Willemsen; Frans P M Cremers; Bert B A de Vries
Journal:  BMC Ophthalmol       Date:  2014-05-01       Impact factor: 2.209

  5 in total

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