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Articles Published Processes
12/26/2022 6:23:38 PM | Browse: 187 | Download: 556
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Received |
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2022-09-29 15:48 |
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Peer-Review Started |
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2022-09-29 15:50 |
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To Make the First Decision |
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Return for Revision |
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2022-10-31 01:20 |
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Revised |
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2022-11-11 15:04 |
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Second Decision |
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2022-12-07 03:09 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2022-12-08 00:31 |
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Articles in Press |
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2022-12-08 00:31 |
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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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2022-12-13 03:17 |
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Publish the Manuscript Online |
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2022-12-26 18:23 |
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 |
Pediatrics |
Manuscript Type |
Case Report |
Article Title |
Congenital nephrogenic diabetes insipidus arginine vasopressin receptor 2 gene mutation at new site: A case report
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Lu-Lu Yang, Yan Xu, Jian-Li Qiu, Qian-Yi Zhao, Man-Man Li and Hui Shi |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Jian-Li Qiu, MD, PhD, Chief Physician, Department of Pediatrics, The First Affiliated Hospital of Henan University of Chinese Medicine, No. 19 Renmin Road, Jinshui District, Zhengzhou 450000, Henan Province, China. qiujianli@126.com |
Key Words |
Congenital nephrogenic diabetes insipidus; Arginine vasopressin receptor 2 gene mutation; New site; Diarrhea; Case report |
Core Tip |
In this case, a pediatric patient with congenital nephrogenic diabetes insipidus harbored a mutation in the arginine vasopressin receptor 2 (AVPR2) gene at a new locus. In addition, the diarrhea observed in this case is likely related to the novel AVPR2 gene mutation. Therefore, the description of new mutations and new manifestations are crucial to complement the clinical deficiencies in the diagnosis of the disease. We report a case harboring an AVPR2 gene mutation at a new locus and a new clinical manifestation. |
Publish Date |
2022-12-26 18:23 |
Citation |
Yang LL, Xu Y, Qiu JL, Zhao QY, Li MM, Shi H. Congenital nephrogenic diabetes insipidus arginine vasopressin receptor 2 gene mutation at new site: A case report. World J Clin Cases 2022; 10(36): 13443-13450 |
URL |
https://www.wjgnet.com/2307-8960/full/v10/i36/13443.htm |
DOI |
https://dx.doi.org/10.12998/wjcc.v10.i36.13443 |
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