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dc.contributor.authorLee, J.Y.L.
dc.contributor.authorLeonard, H.
dc.contributor.authorPiek, Jan Patricia
dc.contributor.authorDowns, Jennepher
dc.date.accessioned2017-01-30T15:31:08Z
dc.date.available2017-01-30T15:31:08Z
dc.date.created2014-03-17T20:01:05Z
dc.date.issued2013
dc.identifier.citationLee, J.Y.L. and Leonard, H. and Piek, J.P. and Downs, J. 2013. Early development and regression in Rett Syndrome. Clinical Genetics. 84 (6): pp. 572-576.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/47088
dc.identifier.doi10.1111/cge.12110
dc.description.abstract

This study utilized developmental profiling to examine symptoms in 14 girls with genetically confirmed Rett syndrome and whose families were participating in the Australian Rett syndrome or InterRett database. Regression was mostly characterized by loss of hand and/or communication skills (13/14) except one girl demonstrated slowing of skill development. Social withdrawal and inconsolable crying often developed simultaneously (9/14), with social withdrawal for shorter duration than inconsolable crying. Previously acquired gross motor skills declined in just over half of the sample (8/14), mostly observed as a loss of balance. Early abnormalities such as vomiting and strabismus were also seen. Our findings provide additional insight into the early clinical profile of Rett syndrome.

dc.publisherWiley-Blackwell Publishing, Inc.
dc.subjectRett syndrome
dc.subjectdevelopment
dc.subjectautistic symptoms
dc.subjectMECP2
dc.subjectregression
dc.titleEarly development and regression in Rett Syndrome
dc.typeJournal Article
dcterms.source.volume84
dcterms.source.startPage572
dcterms.source.endPage576
dcterms.source.issn0009-9163
dcterms.source.titleClinical Genetics
curtin.note

This is the accepted version of the following article: Lee, J.Y.L. and Leonard, H. and Piek, J.P. and Downs, J. 2013. Early development and regression in Rett syndrome. Clinical Genetics. 84 (6): pp. 572-576, which has been published in final form at http://dx.doi.org/10.1111/cge.12110

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curtin.accessStatusOpen access


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