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Articles Published Processes
9/16/2022 11:52:44 AM | Browse: 365 | Download: 1133
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Received |
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2022-05-21 15:19 |
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Peer-Review Started |
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2022-05-21 15:20 |
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To Make the First Decision |
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Return for Revision |
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2022-07-29 02:38 |
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Revised |
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2022-08-12 00:42 |
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Second Decision |
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2022-08-19 03:10 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2022-08-21 17:53 |
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Articles in Press |
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2022-08-21 17:53 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2022-09-02 06:20 |
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Publish the Manuscript Online |
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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
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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 |
Neuroimaging |
Manuscript Type |
Case Report |
Article Title |
Familial mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome: Three case reports
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Xiao Yang and Le-Jun Fu |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Le-Jun Fu, MM, Doctor, 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 |
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