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Behavior and cognitive functioning in Witteveen–Kolk syndrome
Witteveen–Kolk syndrome (WITKOS) is a rare neurodevelopmental disorder characterized by developmental delay/intellectual disability, facial dysmorphisms, and short stature. The syndrome is caused by loss of function of switch‐insensitive 3 transcription regulator family member A (SIN3A). Regarding b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540409/ https://www.ncbi.nlm.nih.gov/pubmed/32783353 http://dx.doi.org/10.1002/ajmg.a.61775 |
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author | van Dongen, Linde C. M. Wingbermühle, Ellen Dingemans, Alexander J. M. Bos‐Roubos, Anja G. Vermeulen, Karlijn Pop‐Purceleanu, Monica Kleefstra, Tjitske Egger, Jos I. M. |
author_facet | van Dongen, Linde C. M. Wingbermühle, Ellen Dingemans, Alexander J. M. Bos‐Roubos, Anja G. Vermeulen, Karlijn Pop‐Purceleanu, Monica Kleefstra, Tjitske Egger, Jos I. M. |
author_sort | van Dongen, Linde C. M. |
collection | PubMed |
description | Witteveen–Kolk syndrome (WITKOS) is a rare neurodevelopmental disorder characterized by developmental delay/intellectual disability, facial dysmorphisms, and short stature. The syndrome is caused by loss of function of switch‐insensitive 3 transcription regulator family member A (SIN3A). Regarding behavioral functioning, Autism Spectrum Disorders (ASD), obsessive–compulsive behaviors, as well as Attention‐Deficit/Hyperactivity Disorder symptoms (ADHD) have been suggested. The present study explores various aspects of neurocognitive functioning in five individuals (age range 10–23) with WITKOS. Medical records and results of extensive neuropsychological assessment are used to describe developmental trajectories and neurocognitive profiles. Systematic analysis of medical records displays developmental difficulties described as ASD or ADHD in childhood, sleep problems and internalizing problems during adolescence. Results of cognitive assessments indicate profoundly disabled (n = 1), mildly disabled (n = 2), borderline (n = 1), and average (n = 1) levels of intelligence. Furthermore, results indicate weaknesses in speed of information processing/sustained attention in all participants, and difficulties in planning and maintaining overview in three participants. Furthermore, parent reports of behavioral functioning primarily suggest problems in social functioning. Implications of both cognitive problems and social–emotional vulnerabilities for counseling are discussed and supplemented with suggestions for interventions. |
format | Online Article Text |
id | pubmed-7540409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75404092020-10-09 Behavior and cognitive functioning in Witteveen–Kolk syndrome van Dongen, Linde C. M. Wingbermühle, Ellen Dingemans, Alexander J. M. Bos‐Roubos, Anja G. Vermeulen, Karlijn Pop‐Purceleanu, Monica Kleefstra, Tjitske Egger, Jos I. M. Am J Med Genet A Clinical Reports Witteveen–Kolk syndrome (WITKOS) is a rare neurodevelopmental disorder characterized by developmental delay/intellectual disability, facial dysmorphisms, and short stature. The syndrome is caused by loss of function of switch‐insensitive 3 transcription regulator family member A (SIN3A). Regarding behavioral functioning, Autism Spectrum Disorders (ASD), obsessive–compulsive behaviors, as well as Attention‐Deficit/Hyperactivity Disorder symptoms (ADHD) have been suggested. The present study explores various aspects of neurocognitive functioning in five individuals (age range 10–23) with WITKOS. Medical records and results of extensive neuropsychological assessment are used to describe developmental trajectories and neurocognitive profiles. Systematic analysis of medical records displays developmental difficulties described as ASD or ADHD in childhood, sleep problems and internalizing problems during adolescence. Results of cognitive assessments indicate profoundly disabled (n = 1), mildly disabled (n = 2), borderline (n = 1), and average (n = 1) levels of intelligence. Furthermore, results indicate weaknesses in speed of information processing/sustained attention in all participants, and difficulties in planning and maintaining overview in three participants. Furthermore, parent reports of behavioral functioning primarily suggest problems in social functioning. Implications of both cognitive problems and social–emotional vulnerabilities for counseling are discussed and supplemented with suggestions for interventions. John Wiley & Sons, Inc. 2020-08-11 2020-10 /pmc/articles/PMC7540409/ /pubmed/32783353 http://dx.doi.org/10.1002/ajmg.a.61775 Text en © 2020 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Clinical Reports van Dongen, Linde C. M. Wingbermühle, Ellen Dingemans, Alexander J. M. Bos‐Roubos, Anja G. Vermeulen, Karlijn Pop‐Purceleanu, Monica Kleefstra, Tjitske Egger, Jos I. M. Behavior and cognitive functioning in Witteveen–Kolk syndrome |
title | Behavior and cognitive functioning in Witteveen–Kolk syndrome |
title_full | Behavior and cognitive functioning in Witteveen–Kolk syndrome |
title_fullStr | Behavior and cognitive functioning in Witteveen–Kolk syndrome |
title_full_unstemmed | Behavior and cognitive functioning in Witteveen–Kolk syndrome |
title_short | Behavior and cognitive functioning in Witteveen–Kolk syndrome |
title_sort | behavior and cognitive functioning in witteveen–kolk syndrome |
topic | Clinical Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540409/ https://www.ncbi.nlm.nih.gov/pubmed/32783353 http://dx.doi.org/10.1002/ajmg.a.61775 |
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