Hostname: page-component-848d4c4894-8kt4b Total loading time: 0 Render date: 2024-06-19T22:53:28.923Z Has data issue: false hasContentIssue false

Gait function in newly diagnosed children with autism: cerebellar and basal ganglia related motor disorder

Published online by Cambridge University Press:  18 September 2006

Nicole J Rinehart
Affiliation:
Centre for Developmental Psychiatry, School of Psychology, Psychiatry, and Psychological Medicine, Monash University, Clayton, Australia.
Bruce J Tonge
Affiliation:
Centre for Developmental Psychiatry, School of Psychology, Psychiatry, and Psychological Medicine, Monash University, Clayton, Australia.
Robert Iansek
Affiliation:
Monash Ageing Research Centre, Geriatric Research Unit, Kingston Centre, Southern Health, Cheltenham, Australia.
Jenny McGinley
Affiliation:
Gait CCRE, Murdoch Childrens Research Institute, Parkville, Australia.
Avril V Brereton
Affiliation:
Centre for Developmental Psychiatry, School of Psychology, Psychiatry, and Psychological Medicine, Monash University, Clayton, Australia.
Peter G Enticott
Affiliation:
Centre for Developmental Psychiatry, School of Psychology, Psychiatry, and Psychological Medicine, Monash University, Clayton, Australia.
John L Bradshaw
Affiliation:
School of Psychology, Psychiatry, and Psychological Medicine, Monash University, Clayton, Victoria, Australia.
Get access

Abstract

We investigated gait in newly diagnosed children with autism. From our previous study with 6- to 14-year-olds, we hypothesized that motor symptoms indicative of basal ganglia and cerebellar dysfunction would appear across the developmental trajectory of autism. Two groups were recruited: children with autism (eight males, three females; mean age 5y 10mo [SD 9mo]; range 4y 4mo–6y 9mo) and a comparison group of typically developing children (eight males, three females; mean age 5y 9mo [SD 1y 1mo]; range 4y 3mo–7y 2mo). The GAITRite Walkway was used to gather data from average gait and intra-walk measurements. Experienced physiotherapists analyzed gait qualitatively. Groups were matched according to age, height, weight, and IQ; although not statistically significant, IQ was lower in the group with autism. Spatiotemporal gait data for children with autism were compatible with findings from patients with cerebellar ataxia: specifically, greater difficulty walking along a straight line, and the coexistence of variable stride length and duration. Children with autism were also less coordinated and rated as more variable and inconsistent (i.e. reduced smoothness) relative to the comparison group. Postural abnormalities in the head and trunk suggest additional involvement of the fronto-striatal basal ganglia region. Abnormal gait features are stable across key developmental periods and are, therefore, promising for use in clinical screening for autism.

Type
Original Articles
Copyright
2006 Mac Keith Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)