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Articles Published Processes
1/12/2022 4:01:56 AM | Browse: 236 | Download: 648
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Received |
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2021-07-10 14:22 |
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Peer-Review Started |
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2021-07-10 14:24 |
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To Make the First Decision |
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Return for Revision |
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2021-10-22 01:02 |
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Revised |
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2021-11-03 03:24 |
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Second Decision |
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2021-12-02 03:26 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-12-03 06:53 |
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Articles in Press |
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2021-12-03 06:53 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2021-11-28 13:54 |
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Typeset the Manuscript |
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2021-12-29 07:54 |
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Publish the Manuscript Online |
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2022-01-12 04:01 |
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 |
Neurosciences |
Manuscript Type |
Case Report |
Article Title |
Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Xin Huang and Dong-Sheng Fan |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Dong-Sheng Fan, MD, PhD, Director, Director, Professor, Department of Neurology, Peking University Third Hospital, Huayuan Bei Lu 49, Haidian District, Beijing, China, Beijing 100191, China. dsfan2010@aliyun.com |
Key Words |
Spinocerebellar ataxia; Recessive; VPS13D gene; Compound heterozygous mutation; Case report |
Core Tip |
We report a female Chinese patient diagnosed with autosomal recessive spinocerebellar ataxia type 4 (SCAR4) with a compound heterozygous mutation, c.3288delA (p.Asp1097ThrfsTer6), in the VPS13D gene. By reviewing the literature, we speculate that the mutation may cause SCAR4 by affecting mitochondrial function. However, there is currently no specific treatment for SCAR4. |
Publish Date |
2022-01-12 04:01 |
Citation |
Huang X, Fan DS. Autosomal recessive spinocerebellar ataxia type 4 with a VPS13D mutation: A case report. World J Clin Cases 2022; 10(2): 703-708 |
URL |
https://www.wjgnet.com/2307-8960/full/v10/i2/703.htm |
DOI |
https://dx.doi.org/10.12998/wjcc.v10.i2.703 |
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