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The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing

Attention-deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders. Several studies have confirmed the co-existence of other neuropsychiatric disorders with ADHD. Out of 106 individuals suspected to have ADHD, eight Saudi Arabian pediatric patients were diagnosed...

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Autores principales: Bogari, Neda M., Al-Allaf, Faisal A., Aljohani, Ashwag, Taher, Mohiuddin M., Qutub, Nermeen A., Alhelfawi, Suhair, Alobaidi, Amal, Alqudah, Derar M., Banni, Hussain, Dairi, Ghida, Amin, Amr A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770135/
https://www.ncbi.nlm.nih.gov/pubmed/33384710
http://dx.doi.org/10.3389/fgene.2020.548559
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author Bogari, Neda M.
Al-Allaf, Faisal A.
Aljohani, Ashwag
Taher, Mohiuddin M.
Qutub, Nermeen A.
Alhelfawi, Suhair
Alobaidi, Amal
Alqudah, Derar M.
Banni, Hussain
Dairi, Ghida
Amin, Amr A.
author_facet Bogari, Neda M.
Al-Allaf, Faisal A.
Aljohani, Ashwag
Taher, Mohiuddin M.
Qutub, Nermeen A.
Alhelfawi, Suhair
Alobaidi, Amal
Alqudah, Derar M.
Banni, Hussain
Dairi, Ghida
Amin, Amr A.
author_sort Bogari, Neda M.
collection PubMed
description Attention-deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders. Several studies have confirmed the co-existence of other neuropsychiatric disorders with ADHD. Out of 106 individuals suspected to have ADHD, eight Saudi Arabian pediatric patients were diagnosed with ADHD using a dual assessment procedure based on highly significant scores from the international criteria for diagnosis; (full form DMS) DSM-5. Then, these patients were examined for the co-existence of autism and ADHD using different international diagnostic protocols. Four patients with combined ADHD and autism and four ADHD patients without autism were examined for the presence of genetic variants. Six variants (chr1:98165091, chr6:32029183, chr6:32035603, chr6:32064098, chr8:2909992, chr16:84213434) were identified in 75% of the patients with ADHD and autism, indicating that these genes may have a possible role in causing autism. Five variants (The chr2:116525960, chr15:68624396, chr15:91452595, chr15:92647645, and chr16:82673047) may increase to the severity of ADHD. This study recommends screening these eleven variants in ADHD cases and their relevant controls to confirm the prevalence in the Saudi population. It is recommended that future studies examine the 11 variants in detail.
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spelling pubmed-77701352020-12-30 The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing Bogari, Neda M. Al-Allaf, Faisal A. Aljohani, Ashwag Taher, Mohiuddin M. Qutub, Nermeen A. Alhelfawi, Suhair Alobaidi, Amal Alqudah, Derar M. Banni, Hussain Dairi, Ghida Amin, Amr A. Front Genet Genetics Attention-deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders. Several studies have confirmed the co-existence of other neuropsychiatric disorders with ADHD. Out of 106 individuals suspected to have ADHD, eight Saudi Arabian pediatric patients were diagnosed with ADHD using a dual assessment procedure based on highly significant scores from the international criteria for diagnosis; (full form DMS) DSM-5. Then, these patients were examined for the co-existence of autism and ADHD using different international diagnostic protocols. Four patients with combined ADHD and autism and four ADHD patients without autism were examined for the presence of genetic variants. Six variants (chr1:98165091, chr6:32029183, chr6:32035603, chr6:32064098, chr8:2909992, chr16:84213434) were identified in 75% of the patients with ADHD and autism, indicating that these genes may have a possible role in causing autism. Five variants (The chr2:116525960, chr15:68624396, chr15:91452595, chr15:92647645, and chr16:82673047) may increase to the severity of ADHD. This study recommends screening these eleven variants in ADHD cases and their relevant controls to confirm the prevalence in the Saudi population. It is recommended that future studies examine the 11 variants in detail. Frontiers Media S.A. 2020-12-15 /pmc/articles/PMC7770135/ /pubmed/33384710 http://dx.doi.org/10.3389/fgene.2020.548559 Text en Copyright © 2020 Bogari, Al-Allaf, Aljohani, Taher, Qutub, Alhelfawi, Alobaidi, Alqudah, Banni, Dairi and Amin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Bogari, Neda M.
Al-Allaf, Faisal A.
Aljohani, Ashwag
Taher, Mohiuddin M.
Qutub, Nermeen A.
Alhelfawi, Suhair
Alobaidi, Amal
Alqudah, Derar M.
Banni, Hussain
Dairi, Ghida
Amin, Amr A.
The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
title The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
title_full The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
title_fullStr The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
title_full_unstemmed The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
title_short The Co-existence of ADHD With Autism in Saudi Children: An Analysis Using Next-Generation DNA Sequencing
title_sort co-existence of adhd with autism in saudi children: an analysis using next-generation dna sequencing
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770135/
https://www.ncbi.nlm.nih.gov/pubmed/33384710
http://dx.doi.org/10.3389/fgene.2020.548559
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