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dc.contributor.authorUrbanowicz, A.
dc.contributor.authorDowns, Jennepher
dc.contributor.authorGirdler, S.
dc.contributor.authorCiccone, N.
dc.contributor.authorLeonard, H.
dc.identifier.citationUrbanowicz, A. and Downs, J. and Girdler, S. and Ciccone, N. and Leonard, H. 2015. Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome. American Journal of Medical Genetics, Part A. 167 (2): pp. 354-362.

This study investigates relationships between methyl-CpG-binding protein 2 gene (MECP2) mutation type and speech-language abilities in girls with Rett syndrome. Cross-sectional data on 766 girls, aged 15 years and under, with genetically confirmed Rett syndrome was obtained from the Australian Rett Syndrome Database (ARSD) (n=244) and the International Rett Syndrome Phenotype Database (InterRett) (n=522). Relationships between MECP2 mutation type and age of regression in speech-language abilities, and the level of speech-language abilities before and after this regression were investigated. The females had a median age of 4.95 years in the ARSD and 5.25 years in InterRett. The majority (89%, 685/766) acquired speech-language abilities in the form of babble or words at some point in time. Of those who acquired babble or words, 85% (581/685) experienced a regression in these abilities. Those with a p.Arg133Cys mutation were the most likely to use one or more words, prior to (RRR=3.45; 95% CI 1.15-10.41) and after (RRR=5.99; 95% CI 2.00-17.92), speech-language regression. Girls with Rett syndrome vary in their use of speech and language, and in their experience of speech-language regression and these variations are partly explained by genotype.

dc.titleAspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome
dc.typeJournal Article
dcterms.source.titleAmerican Journal of Medical Genetics, Part A
curtin.departmentSchool of Physiotherapy and Exercise Science
curtin.accessStatusFulltext not available

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