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9/16/2022 11:52:44 AM | Browse: 208 | Download: 674
Publication Name World Journal of Clinical Cases
Manuscript ID 77809
Country/Territory China
Received
2022-05-21 15:19
Peer-Review Started
2022-05-21 15:20
To Make the First Decision
Return for Revision
2022-07-29 02:38
Revised
2022-08-12 00:42
Second Decision
2022-08-19 03:10
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2022-08-21 17:53
Articles in Press
2022-08-21 17:53
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2022-09-02 06:20
Publish the Manuscript Online
2022-09-16 11:52
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) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Neuroimaging
Manuscript Type Case Report
Article Title Familial mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome: Three case reports
Manuscript Source Unsolicited Manuscript
All Author List Xiao Yang and Le-Jun Fu
ORCID
Author(s) ORCID Number
Xiao Yang http://orcid.org/0000-0001-8453-5608
Le-Jun Fu http://orcid.org/0000-0003-0924-360X
Funding Agency and Grant Number
Corresponding Author Le-Jun Fu, MM, Doctor, Department of Medical Imaging, Tianjin Huanhu Hospital, No. 6 Jizhao Road, Jinnan District, Tianjin 300350, China. doctorfu20220505@163.com
Key Words Mitochondrial encephalomyopathy; Magnetic resonance imaging; Genetic testing; Pathological results; Case report
Core Tip Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode (MELAS) syndrome is a hereditary metabolic disease with complex clinical manifestations, and is often misdiagnosed as cerebral infarction and encephalitis. When the patient has a family history of this disease, blood lactate level is higher than normal, and imaging examination suggests MELAS syndrome, the possibility of MELAS syndrome should be considered. The diagnosis should be confirmed by muscle biopsy and genetic testing.
Publish Date 2022-09-16 11:52
Citation Yang X, Fu LJ. Familial mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome: Three case reports. World J Clin Cases 2022; 10(27): 9945-9953
URL https://www.wjgnet.com/2307-8960/full/v10/i27/9945.htm
DOI https://dx.doi.org/10.12998/wjcc.v10.i27.9945
Full Article (PDF) WJCC-10-9945.pdf
Full Article (Word) WJCC-10-9945.docx
CARE Checklist–2016 77809-CARE-Checklist–2016-revision.pdf
Manuscript File 77809_Auto_Edited-LS.docx
Answering Reviewers 77809-Answering reviewers.pdf
Audio Core Tip 77809-Audio core tip.m4a
Conflict-of-Interest Disclosure Form 77809-Conflict-of-interest statement.pdf
Copyright License Agreement 77809-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s) 77809-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate 77809-Language certificate.pdf
Peer-review Report 77809-Peer-review(s).pdf
Scientific Misconduct Check 77809-Bing-Wu YXJ-2.png
Scientific Editor Work List 77809-Scientific editor work list.pdf