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Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities

BACKGROUND: Relative to other aspects of Down syndrome, remarkably little is known about the psychiatric problems experienced by youth and young adults with this syndrome and if these problems differ from others with intellectual disabilities. Yet adolescence and young adulthood are particularly vul...

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Autores principales: Dykens, Elisabeth M, Shah, Bhavik, Davis, Bruce, Baker, Courtney, Fife, Taylor, Fitzpatrick, Jeri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373108/
https://www.ncbi.nlm.nih.gov/pubmed/25810793
http://dx.doi.org/10.1186/s11689-015-9101-1
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author Dykens, Elisabeth M
Shah, Bhavik
Davis, Bruce
Baker, Courtney
Fife, Taylor
Fitzpatrick, Jeri
author_facet Dykens, Elisabeth M
Shah, Bhavik
Davis, Bruce
Baker, Courtney
Fife, Taylor
Fitzpatrick, Jeri
author_sort Dykens, Elisabeth M
collection PubMed
description BACKGROUND: Relative to other aspects of Down syndrome, remarkably little is known about the psychiatric problems experienced by youth and young adults with this syndrome and if these problems differ from others with intellectual disabilities. Yet adolescence and young adulthood are particularly vulnerable time periods, as they involve multiple life transitions in educational, medical, and other service systems. METHODS: This study compared the psychiatric diagnoses of 49 adolescent and young adult patients with Down syndrome to 70 patients with other intellectual disabilities (IDs). The groups were similar in age, gender, and level of intellectual impairment. The 119 participants, aged 13 to 29 years (M = 21) were evaluated in one of two specialized psychiatric clinics. RESULTS: In contrast to previous literature, those with Down syndrome versus other IDs had significantly higher rates of psychosis NOS or depression with psychotic features (43% versus 13%). Unlike the ID group, psychosis was predominantly seen in females with Down syndrome. Marked motoric slowing in performing routine daily activities or in expressive language was manifested in 17% of patients with Down syndrome. No group differences were found in anxiety or depressive disorders, and the ID group had significantly higher rates of bipolar and impulse control disorders. CONCLUSIONS: These preliminary observations warrant further studies on genetic, neurological, and psychosocial factors that place some young people with Down syndrome or other IDs at high risk for severe psychiatric illness.
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spelling pubmed-43731082015-03-26 Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities Dykens, Elisabeth M Shah, Bhavik Davis, Bruce Baker, Courtney Fife, Taylor Fitzpatrick, Jeri J Neurodev Disord Research BACKGROUND: Relative to other aspects of Down syndrome, remarkably little is known about the psychiatric problems experienced by youth and young adults with this syndrome and if these problems differ from others with intellectual disabilities. Yet adolescence and young adulthood are particularly vulnerable time periods, as they involve multiple life transitions in educational, medical, and other service systems. METHODS: This study compared the psychiatric diagnoses of 49 adolescent and young adult patients with Down syndrome to 70 patients with other intellectual disabilities (IDs). The groups were similar in age, gender, and level of intellectual impairment. The 119 participants, aged 13 to 29 years (M = 21) were evaluated in one of two specialized psychiatric clinics. RESULTS: In contrast to previous literature, those with Down syndrome versus other IDs had significantly higher rates of psychosis NOS or depression with psychotic features (43% versus 13%). Unlike the ID group, psychosis was predominantly seen in females with Down syndrome. Marked motoric slowing in performing routine daily activities or in expressive language was manifested in 17% of patients with Down syndrome. No group differences were found in anxiety or depressive disorders, and the ID group had significantly higher rates of bipolar and impulse control disorders. CONCLUSIONS: These preliminary observations warrant further studies on genetic, neurological, and psychosocial factors that place some young people with Down syndrome or other IDs at high risk for severe psychiatric illness. BioMed Central 2015-03-01 2015 /pmc/articles/PMC4373108/ /pubmed/25810793 http://dx.doi.org/10.1186/s11689-015-9101-1 Text en © Dykens et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dykens, Elisabeth M
Shah, Bhavik
Davis, Bruce
Baker, Courtney
Fife, Taylor
Fitzpatrick, Jeri
Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities
title Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities
title_full Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities
title_fullStr Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities
title_full_unstemmed Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities
title_short Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities
title_sort psychiatric disorders in adolescents and young adults with down syndrome and other intellectual disabilities
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373108/
https://www.ncbi.nlm.nih.gov/pubmed/25810793
http://dx.doi.org/10.1186/s11689-015-9101-1
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