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1/18/2024 9:11:52 AM | Browse: 113 | Download: 527
Publication Name World Journal of Clinical Cases
Manuscript ID 88346
Country China
Received
2023-09-21 04:55
Peer-Review Started
2023-09-21 04:57
To Make the First Decision
Return for Revision
2023-11-20 07:55
Revised
2023-12-04 23:44
Second Decision
2024-01-04 02:49
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2024-01-04 07:53
Articles in Press
2024-01-04 07:53
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-01-11 06:16
Publish the Manuscript Online
2024-01-18 09:11
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) 2024. 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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Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Clinical Neurology
Manuscript Type Case Report
Article Title Special electromyographic features in a child with paramyotonia congenita: A case report and review of literature
Manuscript Source Unsolicited Manuscript
All Author List Hui Yi, Chen-Xiang Liu, Shu-Xin Ye and Yu-Lin Liu
ORCID
Author(s) ORCID Number
Hui Yi http://orcid.org/0009-0009-2203-5451
Chen-Xiang Liu http://orcid.org/0009-0007-3756-9507
Shu-Xin Ye http://orcid.org/0000-0002-6342-3348
Yu-Lin Liu http://orcid.org/0009-0001-9136-0022
Funding Agency and Grant Number
Corresponding Author Yu-Lin Liu, MA, Deputy Director, Department of Neuroelectrophysiology, Qilu Children’s Hospital of Shandong University, No. 23976 Jingshi Road, Jinan 250000, Shandong Province, China. liuyulin1122@126.com
Key Words Paramyotonia congenita; Channelopathy; Electromyography; Child; Case report
Core Tip Paramyotonia congenita (PMC) is a rare sodium channelopathy of skeletal muscle, first identified by Eulenburg. The distinguishing feature of PMC is paradoxical myotonia, where myotonia worsens with cold and exercise. In instances where genetic testing is unavailable, electromyographic (EMG) is a swift, cost-effective diagnostic and differential diagnostic method for PMC. This article elaborates on the EMG characteristics of a recently diagnosed PMC case at our hospital. In this particular case revealed the two types of myotonic discharges, and had not been documented in other studies. We underscore two distinctive features: Giant-amplitude potentials and irregular waves.
Publish Date 2024-01-18 09:11
Citation Yi H, Liu CX, Ye SX, Liu YL. Special electromyographic features in a child with paramyotonia congenita: A case report and review of literature. World J Clin Cases 2024; 12(3): 587-595
URL https://www.wjgnet.com/2307-8960/full/v12/i3/587.htm
DOI https://dx.doi.org/10.12998/wjcc.v12.i3.587
Full Article (PDF) WJCC-12-587-with-cover.pdf
Full Article (Word) WJCC-12-587.docx
CARE Checklist–2016 88346-CARE Checklist (2016).pdf
Manuscript File 88346_Auto_Edited-YJP.docx
Answering Reviewers 88346-Answering reviewers.pdf
Audio Core Tip 88346-Audio core tip.mp3
Conflict-of-Interest Disclosure Form 88346-Conflict-of-interest statement.pdf
Copyright License Agreement 88346-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s) 88346-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate 88346-Language certificate.pdf
Peer-review Report 88346-Peer-review(s).pdf
Scientific Misconduct Check 88346-Bing-Wang JJ-2.png
Scientific Editor Work List 88346-Scientific editor work list.pdf
CrossCheck Report 88346-CrossCheck report.pdf