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dc.contributor.authorDowns, Jennepher
dc.contributor.authorBebbington, A.
dc.contributor.authorKaufmann, W.
dc.contributor.authorLeonard, H.
dc.date.accessioned2017-01-30T12:37:30Z
dc.date.available2017-01-30T12:37:30Z
dc.date.created2014-05-25T20:00:32Z
dc.date.issued2011
dc.identifier.citationDowns, J. and Bebbington, A. and Kaufmann, W. and Leonard, H. 2011. Longitudinal hand function in Rett syndrome. Journal of Child Neurology. 26 (3): pp. 334-340.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/23479
dc.identifier.doi10.1177/0883073810381920
dc.description.abstract

Loss of hand function is a core feature of Rett syndrome. This article describes longitudinal hand function at 3 time points for 72 subjects participating in the Australian Rett Syndrome Database. Approximately 40% of subjects with some grasping abilities lost skill over the 3- to 4-year period between video assessments. In these subjects, a decrease in hand function was seen less frequently in girls 13 to 19 years old than in those younger than 8 years, in subjects with some mobility compared with those who were wheelchair bound, and in those who had previously been able to finger feed. Relationships with the magnitude of change reflected these findings. Change in hand function did not vary with clinical severity. The results for all subjects were similar to results obtained when analysis was restricted to those with a pathogenic mutation. Variability in the longitudinal course of hand function in Rett syndrome was observed.

dc.publisherSage Publications, Inc.
dc.subjectRett syndrome
dc.subjecthand function
dc.subjectMECP2
dc.subjectphenotype
dc.subjectlongitudinal
dc.titleLongitudinal hand function in Rett syndrome
dc.typeJournal Article
dcterms.source.volume26
dcterms.source.number3
dcterms.source.startPage334
dcterms.source.endPage340
dcterms.source.issn0883-0738
dcterms.source.titleJournal of Child Neurology
curtin.department
curtin.accessStatusFulltext not available


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