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22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report
22q11.2 Deletion Syndrome (22q11 DS) is a multisystemic condition that may also include neuropsychiatric disorders. We present a case of a 15-year-old boy that was evaluated for social difficulties, and anxiety with the above genetic abnormality. Clinical features were rather complex as different ne...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601501/ https://www.ncbi.nlm.nih.gov/pubmed/23519073 http://dx.doi.org/10.4021/jocmr1222w |
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author | Scandurra, Valeria Scordo, Maria R. Canitano, Roberto de Bruin, Esther I. |
author_facet | Scandurra, Valeria Scordo, Maria R. Canitano, Roberto de Bruin, Esther I. |
author_sort | Scandurra, Valeria |
collection | PubMed |
description | 22q11.2 Deletion Syndrome (22q11 DS) is a multisystemic condition that may also include neuropsychiatric disorders. We present a case of a 15-year-old boy that was evaluated for social difficulties, and anxiety with the above genetic abnormality. Clinical features were rather complex as different neuropsychiatric symptoms emerged from assessment and clinical evaluation. As a result we propose that Multiple Complex Developmental Disorder (MCDD) would be the best fitting comprehensive diagnosis to be added to the DSM-IV category of Pervasive Developmental Disorder-Not Otherwise Specified. |
format | Online Article Text |
id | pubmed-3601501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36015012013-03-21 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report Scandurra, Valeria Scordo, Maria R. Canitano, Roberto de Bruin, Esther I. J Clin Med Res Case Report 22q11.2 Deletion Syndrome (22q11 DS) is a multisystemic condition that may also include neuropsychiatric disorders. We present a case of a 15-year-old boy that was evaluated for social difficulties, and anxiety with the above genetic abnormality. Clinical features were rather complex as different neuropsychiatric symptoms emerged from assessment and clinical evaluation. As a result we propose that Multiple Complex Developmental Disorder (MCDD) would be the best fitting comprehensive diagnosis to be added to the DSM-IV category of Pervasive Developmental Disorder-Not Otherwise Specified. Elmer Press 2013-04 2013-02-25 /pmc/articles/PMC3601501/ /pubmed/23519073 http://dx.doi.org/10.4021/jocmr1222w Text en Copyright 2013, Scandurra et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Scandurra, Valeria Scordo, Maria R. Canitano, Roberto de Bruin, Esther I. 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report |
title | 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report |
title_full | 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report |
title_fullStr | 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report |
title_full_unstemmed | 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report |
title_short | 22q11 Deletion Syndrome and Multiple Complex Developmental Disorder: A Case Report |
title_sort | 22q11 deletion syndrome and multiple complex developmental disorder: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601501/ https://www.ncbi.nlm.nih.gov/pubmed/23519073 http://dx.doi.org/10.4021/jocmr1222w |
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