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The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes
Psychopathology is prevalent in Williams (WS), fragile X (FXS) and Prader–Willi (PWS) syndromes. However, little is known about the potential correlates of psychopathology in these groups. A questionnaire study was completed by 111 caregivers of individuals with WS (n = 35); FXS (n = 50) and PWS (n ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010621/ https://www.ncbi.nlm.nih.gov/pubmed/31802317 http://dx.doi.org/10.1007/s10803-019-04317-1 |
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author | Royston, R. Oliver, C. Howlin, P. Dosse, A. Armitage, P. Moss, J. Waite, J. |
author_facet | Royston, R. Oliver, C. Howlin, P. Dosse, A. Armitage, P. Moss, J. Waite, J. |
author_sort | Royston, R. |
collection | PubMed |
description | Psychopathology is prevalent in Williams (WS), fragile X (FXS) and Prader–Willi (PWS) syndromes. However, little is known about the potential correlates of psychopathology in these groups. A questionnaire study was completed by 111 caregivers of individuals with WS (n = 35); FXS (n = 50) and PWS (n = 26). Mean age was 26 years (range 12–57 years); 74 (67%) were male. Multiple regression analyses indicated that higher rates of health problems and sensory impairments predicted higher psychopathology in WS (p < .0001). In PWS, poorer adaptive ability predicted higher overall psychiatric disturbance (p = .001), generalised anxiety (p = .006) and hyperactivity (p = .003). There were no significant predictors in FXS. This study highlights dissociations in the potential risk markers of psychopathology between genetic syndromes. Implications for intervention are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10803-019-04317-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7010621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-70106212020-02-24 The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes Royston, R. Oliver, C. Howlin, P. Dosse, A. Armitage, P. Moss, J. Waite, J. J Autism Dev Disord Original Paper Psychopathology is prevalent in Williams (WS), fragile X (FXS) and Prader–Willi (PWS) syndromes. However, little is known about the potential correlates of psychopathology in these groups. A questionnaire study was completed by 111 caregivers of individuals with WS (n = 35); FXS (n = 50) and PWS (n = 26). Mean age was 26 years (range 12–57 years); 74 (67%) were male. Multiple regression analyses indicated that higher rates of health problems and sensory impairments predicted higher psychopathology in WS (p < .0001). In PWS, poorer adaptive ability predicted higher overall psychiatric disturbance (p = .001), generalised anxiety (p = .006) and hyperactivity (p = .003). There were no significant predictors in FXS. This study highlights dissociations in the potential risk markers of psychopathology between genetic syndromes. Implications for intervention are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10803-019-04317-1) contains supplementary material, which is available to authorized users. Springer US 2019-12-04 2020 /pmc/articles/PMC7010621/ /pubmed/31802317 http://dx.doi.org/10.1007/s10803-019-04317-1 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Royston, R. Oliver, C. Howlin, P. Dosse, A. Armitage, P. Moss, J. Waite, J. The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes |
title | The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes |
title_full | The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes |
title_fullStr | The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes |
title_full_unstemmed | The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes |
title_short | The Profiles and Correlates of Psychopathology in Adolescents and Adults with Williams, Fragile X and Prader–Willi Syndromes |
title_sort | profiles and correlates of psychopathology in adolescents and adults with williams, fragile x and prader–willi syndromes |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010621/ https://www.ncbi.nlm.nih.gov/pubmed/31802317 http://dx.doi.org/10.1007/s10803-019-04317-1 |
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