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

• Main Author: Donald, Kirsten Ann Mary
• Other Authors: Wilmshurst, Jo
• Format: Dissertation
• Language: English
• Published: University of Cape Town 2014
• Subjects: Paediatric Neurology
• Online Access: http://hdl.handle.net/11427/10376

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.