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Articles Published Processes
6/11/2021 9:22:18 AM | Browse: 562 | Download: 1582
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Received |
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2020-09-14 01:32 |
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Peer-Review Started |
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2020-09-08 03:11 |
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First Decision by Editorial Office Director |
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2021-01-24 18:54 |
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Return for Revision |
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2021-01-24 18:54 |
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Revised |
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2021-01-27 07:41 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2021-04-15 10:31 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2021-04-19 18:15 |
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Articles in Press |
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2021-04-19 18:15 |
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Edit the Manuscript by Language Editor |
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2021-04-28 06:52 |
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Typeset the Manuscript |
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2021-05-28 07:44 |
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Publish the Manuscript Online |
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2021-06-11 09:22 |
| 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 |
Genetics & Heredity |
| Manuscript Type |
Case Report |
| Article Title |
Alport syndrome combined with lupus nephritis in a Chinese family: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Hui-Fang Liu, Qing Li and You-Qun Peng |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| the Science and Technology Bureau of Jiulongpo District in Chongqing |
2019-02-027-D |
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| Corresponding Author |
You-Qun Peng, PhD, Professor, Department of Nephrology, Traditional Chinese Medicine Hospital of Jiulongpo District, No. 160 Yuquancun Street, Jiulongpo District
, Chongqing 400050, China. 376452999@qq.com |
| Key Words |
Alport syndrome; Lupus nephritis; COL4A3; Whole exome sequencing; Splicing site; Case report |
| Core Tip |
Alport syndrome is a hereditary nephropathy and can be combined with other disease or syndrome. We present the case of a 33-year-old male who was initially diagnosed with lupus nephritis but further diagnosed with Alport syndrome after genetic testing. He achieved complete remission after treatment with hormone and immunosuppressive agent. A variant in the splicing site of intron 22 in the COL4A3 gene was identified by the whole exome sequencing, which was co-segregated with the phenotype in the pedigree. |
| Publish Date |
2021-06-11 09:22 |
| Citation |
Liu HF, Li Q, Peng YQ. Alport syndrome combined with Lupus nephritis in a Chinese family: A case report. World J Clin Cases 2021; 9(18): 4721-4727 |
| URL |
https://www.wjgnet.com/2307-8960/full/v9/i18/4721.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v9.i18.4721 |
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