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Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome

Rett syndrome (RTT) is a developmental disorder characterized by regression of purposeful hand skills and spoken language, although some affected children retain some ability to speech. We assessed the communicative abilities of five young girls, who were later diagnosed with the preserved speech va...

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Autores principales: Marschik, Peter B., Kaufmann, Walter E., Einspieler, Christa, Bartl-Pokorny, Katrin D., Wolin, Thomas, Pini, Giorgio, Budimirovic, Dejan B., Zappella, Michele, Sigafoos, Jeff
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445809/
https://www.ncbi.nlm.nih.gov/pubmed/22699249
http://dx.doi.org/10.1016/j.ridd.2012.04.012
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author Marschik, Peter B.
Kaufmann, Walter E.
Einspieler, Christa
Bartl-Pokorny, Katrin D.
Wolin, Thomas
Pini, Giorgio
Budimirovic, Dejan B.
Zappella, Michele
Sigafoos, Jeff
author_facet Marschik, Peter B.
Kaufmann, Walter E.
Einspieler, Christa
Bartl-Pokorny, Katrin D.
Wolin, Thomas
Pini, Giorgio
Budimirovic, Dejan B.
Zappella, Michele
Sigafoos, Jeff
author_sort Marschik, Peter B.
collection PubMed
description Rett syndrome (RTT) is a developmental disorder characterized by regression of purposeful hand skills and spoken language, although some affected children retain some ability to speech. We assessed the communicative abilities of five young girls, who were later diagnosed with the preserved speech variant of RTT, during the pre-regression period (aged 12–24 months). Videotapes, obtained by parents during routine family situations and celebrations, were analyzed to identify communicative forms and functions used by these toddlers. Non-verbal communicative forms dominated over verbal-communicative forms for six of the eight identified communication functions. Although the girls used various non-verbal forms to make requests, for example, none of the individuals were observed to make choices or request information. Early peculiarities in the speech-language domain during the first year of life became more prominent and evident during the second year of life as general differences between typical development and atypical development become more obvious in RTT. These findings highlight the importance of assessing socio-communicative forms and functions at early age in children with RTT. The results suggest that speech-language functions did not appear to play a major role in the children's communicative attempts. We conclude that, even among children with the preserved speech variant, socio-communicative deficits are present before regression and persist after this period.
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spelling pubmed-34458092012-11-01 Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome Marschik, Peter B. Kaufmann, Walter E. Einspieler, Christa Bartl-Pokorny, Katrin D. Wolin, Thomas Pini, Giorgio Budimirovic, Dejan B. Zappella, Michele Sigafoos, Jeff Res Dev Disabil Article Rett syndrome (RTT) is a developmental disorder characterized by regression of purposeful hand skills and spoken language, although some affected children retain some ability to speech. We assessed the communicative abilities of five young girls, who were later diagnosed with the preserved speech variant of RTT, during the pre-regression period (aged 12–24 months). Videotapes, obtained by parents during routine family situations and celebrations, were analyzed to identify communicative forms and functions used by these toddlers. Non-verbal communicative forms dominated over verbal-communicative forms for six of the eight identified communication functions. Although the girls used various non-verbal forms to make requests, for example, none of the individuals were observed to make choices or request information. Early peculiarities in the speech-language domain during the first year of life became more prominent and evident during the second year of life as general differences between typical development and atypical development become more obvious in RTT. These findings highlight the importance of assessing socio-communicative forms and functions at early age in children with RTT. The results suggest that speech-language functions did not appear to play a major role in the children's communicative attempts. We conclude that, even among children with the preserved speech variant, socio-communicative deficits are present before regression and persist after this period. Pergamon Press 2012-11 /pmc/articles/PMC3445809/ /pubmed/22699249 http://dx.doi.org/10.1016/j.ridd.2012.04.012 Text en © 2012 Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Marschik, Peter B.
Kaufmann, Walter E.
Einspieler, Christa
Bartl-Pokorny, Katrin D.
Wolin, Thomas
Pini, Giorgio
Budimirovic, Dejan B.
Zappella, Michele
Sigafoos, Jeff
Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
title Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
title_full Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
title_fullStr Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
title_full_unstemmed Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
title_short Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
title_sort profiling early socio-communicative development in five young girls with the preserved speech variant of rett syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445809/
https://www.ncbi.nlm.nih.gov/pubmed/22699249
http://dx.doi.org/10.1016/j.ridd.2012.04.012
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