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Articles Published Processes
8/24/2021 2:07:00 AM | Browse: 385 | Download: 952
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Received |
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2021-01-11 08:10 |
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Peer-Review Started |
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2021-01-11 08:11 |
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To Make the First Decision |
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Return for Revision |
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2021-04-25 17:41 |
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Revised |
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2021-05-01 21:55 |
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Second Decision |
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2021-07-05 05:49 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-07-05 06:21 |
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Articles in Press |
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2021-07-05 06:21 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2021-07-14 23:26 |
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Typeset the Manuscript |
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2021-08-16 15:07 |
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Publish the Manuscript Online |
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2021-08-24 02:07 |
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 |
Clinical Neurology |
Manuscript Type |
Case Report |
Article Title |
Idiopathic basal ganglia calcification associated with new MYORG mutation site: A case report
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Bei-Ni Fei, Hui-Zhen Su, Xiang-Ping Yao, Jing Ding and Xin Wang |
ORCID |
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Funding Agency and Grant Number |
Funding Agency |
Grant Number |
National Key R&D Program of China |
2018YFC1312900 |
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Corresponding Author |
Jing Ding, MD, Doctor, Doctor, Department of Neurology, Zhongshan Hospital, Fudan University, No. 180 Fenglin Road, Shanghai 200032, China. ding.jing@zs-hospital.sh.cn |
Key Words |
Idiopathic basal ganglia calcification; Fahr’s disease; Gene; Point mutation; Inheritance; Case report |
Core Tip |
Idiopathic basal ganglia calcification (IBGC) is characterized by calcification of basal ganglia and other regions of the brain. IBGC is clinically heterogeneous and usually exhibits an autosomal dominant pattern of inheritance. We report a case of a 61-year-old man, who presented with symptoms of dysphagia and alalia. His computed tomography scan of the brain revealed bilateral symmetric calcifications of basal ganglia, cerebellum, thalamus and periventricular area. The genetic test showed a new mutation sites of MYORG. |
Publish Date |
2021-08-24 02:07 |
Citation |
Fei BN, Su HZ, Yao XP, Ding J, Wang X. Idiopathic basal ganglia calcification associated with new MYORG mutation site: A case report. World J Clin Cases 2021; 9(24): 7169-7174 |
URL |
https://www.wjgnet.com/2307-8960/full/v9/i24/7169.htm |
DOI |
https://dx.doi.org/10.12998/wjcc.v9.i24.7169 |
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