Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period

Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the MECP2 gene. We describe change in gross motor function over 3 to 4 years for 70 subjects participating in the Australian Rett Syndrome Database. Linear regression was used to assess relationships wit...

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Main Authors: Foley, K., Downs, Jennepher, Bebbington, A., Jacoby, P., Girdler, S., Kaufmann, W., Leonard, H.
Format: Journal Article
Published: Sage 2011
Online Access:http://hdl.handle.net/20.500.11937/3520
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author Foley, K.
Downs, Jennepher
Bebbington, A.
Jacoby, P.
Girdler, S.
Kaufmann, W.
Leonard, H.
author_facet Foley, K.
Downs, Jennepher
Bebbington, A.
Jacoby, P.
Girdler, S.
Kaufmann, W.
Leonard, H.
author_sort Foley, K.
building Curtin Institutional Repository
collection Online Access
description Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the MECP2 gene. We describe change in gross motor function over 3 to 4 years for 70 subjects participating in the Australian Rett Syndrome Database. Linear regression was used to assess relationships with age, genotype, and general and complex gross motor skills scores measured on the Gross Motor Scale for Rett syndrome. Skills were slightly better or maintained in approximately 40% of subjects and slightly decreased in approximately 60%. Teenagers and women who walked in 2004 were less likely to lose complex skills than those younger. Girls with a p.R294X mutation were more likely to lose complex motor skills, otherwise skill changes were spread across the mutation categories. In conclusion, small changes were observed over this period with greater stability of skills in teenagers and women with the ability to walk.
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spelling curtin-20.500.11937-35202017-09-13T16:08:57Z Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period Foley, K. Downs, Jennepher Bebbington, A. Jacoby, P. Girdler, S. Kaufmann, W. Leonard, H. Rett syndrome is a rare but severe neurological disorder typically associated with a mutation in the MECP2 gene. We describe change in gross motor function over 3 to 4 years for 70 subjects participating in the Australian Rett Syndrome Database. Linear regression was used to assess relationships with age, genotype, and general and complex gross motor skills scores measured on the Gross Motor Scale for Rett syndrome. Skills were slightly better or maintained in approximately 40% of subjects and slightly decreased in approximately 60%. Teenagers and women who walked in 2004 were less likely to lose complex skills than those younger. Girls with a p.R294X mutation were more likely to lose complex motor skills, otherwise skill changes were spread across the mutation categories. In conclusion, small changes were observed over this period with greater stability of skills in teenagers and women with the ability to walk. 2011 Journal Article http://hdl.handle.net/20.500.11937/3520 10.1177/0883073811402688 Sage restricted
spellingShingle Foley, K.
Downs, Jennepher
Bebbington, A.
Jacoby, P.
Girdler, S.
Kaufmann, W.
Leonard, H.
Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period
title Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period
title_full Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period
title_fullStr Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period
title_full_unstemmed Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period
title_short Change in Gross Motor Abilities of Girls and Women with Rett Syndrome Over a 3- to 4- Year Period
title_sort change in gross motor abilities of girls and women with rett syndrome over a 3- to 4- year period
url http://hdl.handle.net/20.500.11937/3520