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Articles Published Processes
8/5/2021 2:37:05 PM | Browse: 363 | Download: 855
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Received |
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2021-03-18 02:15 |
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Peer-Review Started |
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2021-03-18 03:04 |
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To Make the First Decision |
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Return for Revision |
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2021-05-11 20:43 |
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Revised |
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2021-05-24 21:42 |
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Second Decision |
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2021-06-15 12:32 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-06-15 13:08 |
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Articles in Press |
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2021-06-15 13:08 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2021-06-23 21:42 |
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Typeset the Manuscript |
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2021-08-02 00:48 |
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Publish the Manuscript Online |
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2021-08-05 14:37 |
| ISSN |
2307-8960 (online) |
| Open Access |
This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Pediatrics |
| Manuscript Type |
Case Report |
| Article Title |
Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Shuang-Zhu Lin, Xin-Yu Zhou, Wan-Qi Wang and Kai Jiang |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| Natural Science Foundation of Jilin Province |
20200201486JC |
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| Corresponding Author |
Kai Jiang, MD, Professor, Department of Diagnosis and Treatment Center for Children, First Affiliated Hospital to Changchun University of Chinese Medicine, No. 1478 Gongnong Road, Chaoyang District, Changchun 130021, Jilin Province, China. 2835221172@qq.com |
| Key Words |
Mental retardation; Developmental retardation; FOXP1; Genetic expression; Case report |
| Core Tip |
We report the characteristic features of autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion. In this case, the FOXP1 gene of the child had a heterozygous deletion variation, and the mutation site was heterozygous deletion in exon 6-21. This study provides a molecular basis for etiological diagnosis and treatment of the child, as well as for genetic counselling for the pedigree. |
| Publish Date |
2021-08-05 14:37 |
| Citation |
Lin SZ, Zhou XY, Wang WQ, Jiang K. Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report. World J Clin Cases 2021; 9(23): 6858-6866 |
| URL |
https://www.wjgnet.com/2307-8960/full/v9/i23/6858.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v9.i23.6858 |
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