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Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype

Includes bibliographical references (leaves 76-82).

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Bibliographic Details
Main Author: Donald, Kirsten Ann Mary
Other Authors: Wilmshurst, Jo
Format: Thesis
Language:English
Published: Department of Paediatrics and Child Health 2014
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access_status_str Open Access
author Donald, Kirsten Ann Mary
author2 Wilmshurst, Jo
author_browse Donald, Kirsten Ann Mary
Wilmshurst, Jo
author_facet Wilmshurst, Jo
Donald, Kirsten Ann Mary
author_sort Donald, Kirsten Ann Mary
collection Thesis
description Includes bibliographical references (leaves 76-82).
format Thesis
id oai:open.uct.ac.za:11427/10376
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:48:52.583Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Paediatrics and Child Health
publisherStr Department of Paediatrics and Child Health
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/10376 Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype Donald, Kirsten Ann Mary Wilmshurst, Jo Thomas, Kevin Paediatric Neurology Includes bibliographical references (leaves 76-82). The spectrum of central nervous system manifestations of DMD is less well described than its musculoskeletal aspects. Although international studies have reported intellectual function ranging from above-average to severe intellectual disability, they have consistently found the average full-scale IQ of affected boys to be reduced by approximately one standard deviation. Fewer reports are available for DMD boys in the pre-school age group. There is also limited data on the behavioural profile of boys with this condition. No material on these aspects of DMD in South African children has been published to date. This pilot case control study aimed to determine the neurocognitive and behavioural phenotype of a cohort of South African children with a confirmed diagnosis of Duchenne muscular dystrophy as compared to the profile of a matched control cohort of children. 2014-12-28T14:55:42Z 2014-12-28T14:55:42Z 2008 Master Thesis Masters MPhil http://hdl.handle.net/11427/10376 eng application/pdf Department of Paediatrics and Child Health Faculty of Health Sciences University of Cape Town
spellingShingle Paediatric Neurology
Donald, Kirsten Ann Mary
Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
thesis_degree_str Master's
title Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
title_full Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
title_fullStr Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
title_full_unstemmed Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
title_short Intellectual and behavioural functioning in boys with Duchenne Muscular Dystrophy : neuropsychological testing and correlation with genotype
title_sort intellectual and behavioural functioning in boys with duchenne muscular dystrophy neuropsychological testing and correlation with genotype
topic Paediatric Neurology
url http://hdl.handle.net/11427/10376
work_keys_str_mv AT donaldkirstenannmary intellectualandbehaviouralfunctioninginboyswithduchennemusculardystrophyneuropsychologicaltestingandcorrelationwithgenotype