Publication Name	World Journal of Clinical Cases
Manuscript ID	98319
Country	China

Received	2024-06-24 10:08
Peer-Review Started	2024-06-24 10:08
To Make the First Decision
Return for Revision	2024-09-15 03:17
Revised	2024-09-25 10:25
Second Decision	2024-10-16 02:46
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2024-10-16 08:38
Articles in Press	2024-10-16 08:38
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2024-10-31 01:07
Publish the Manuscript Online	2024-11-08 03:51

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: https://creativecommons.org/Licenses/by-nc/4.0/
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Category	Pediatrics
Manuscript Type	Editorial
Article Title	Magnetic resonance imaging evaluation and nuclear receptor binding SET domain protein 1 mutation in the Sotos syndrome with attention-deficit/hyperactivity disorder
Manuscript Source	Invited Manuscript
All Author List	Wei Zhu
ORCID	Author(s) ORCID Number Wei Zhu http://orcid.org/0000-0001-7523-7203
Funding Agency and Grant Number	Funding Agency Grant Number Natural Science Foundation of Shanghai No. 17ZR1431400 National Key R and D Program of China No. 2017YFA0103902
Corresponding Author	Wei Zhu, PhD, Shanghai XiRong Information Science and Technology Co., Ltd, National Science and Technology Park, School of Life Sciences and Technology, Tongji University, No. 1239 Siping Road, Yangpu District, Shanghai 200092, China. zhuwei8247@aliyun.com
Key Words	Sotos syndrome; Attention-deficit/hyperactivity disorder; Genetic mutation; Magnetic resonance imaging; Wavelet fusion
Core Tip	Nuclear receptor binding SET domain protein 1 (NSD1) gene mutation has been shown to be involved in the process of Sotos syndrome but without a confirmed effect on patients with attention-deficit/hyperactivity disorder (ADHD). The case report by Yang et al showed a meaningful result to indicate that NSD1 gene mutation existed in a pediatric patient with Sotos syndrome and ADHD.
Publish Date	2024-11-08 03:51
Citation	<p>Zhu W. Magnetic resonance imaging evaluation and nuclear receptor binding SET domain protein 1 mutation in the Sotos syndrome with attention-deficit/hyperactivity disorder. <i>World J Clin Cases</i> 2025; 13(2): 98319</p>
URL	https://www.wjgnet.com/2307-8960/full/v13/i2/98319.htm
DOI	https://dx.doi.org/10.12998/wjcc.v13.i2.98319

Full Article (PDF)	WJCC-13-98319-with-cover.pdf
Manuscript File	98319_Auto_Edited_085738.docx
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