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12/26/2022 6:23:38 PM | Browse: 187 | Download: 556
Publication Name World Journal of Clinical Cases
Manuscript ID 80312
Country China
Received
2022-09-29 15:48
Peer-Review Started
2022-09-29 15:50
To Make the First Decision
Return for Revision
2022-10-31 01:20
Revised
2022-11-11 15:04
Second Decision
2022-12-07 03:09
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2022-12-08 00:31
Articles in Press
2022-12-08 00:31
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2022-12-13 03:17
Publish the Manuscript Online
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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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
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
Author(s) ORCID Number
Yan Xu http://orcid.org/0000-0001-5258-339X
Jian-Li Qiu http://orcid.org/0000-0001-6796-3774
Funding Agency and Grant Number
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
Full Article (PDF) WJCC-10-13443.pdf
Full Article (Word) WJCC-10-13443.docx
Manuscript File 80312_Auto_Edited-JLW.docx
Answering Reviewers 80312-Answering reviewers.pdf
Audio Core Tip 80312-Audio core tip.mp3
Conflict-of-Interest Disclosure Form 80312-Conflict-of-interest statement.pdf
Copyright License Agreement 80312-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s) 80312-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate 80312-Language certificate.pdf
Peer-review Report 80312-Peer-review(s).pdf
Scientific Misconduct Check 80312-Bing-Wang JJ-2.png
Scientific Editor Work List 80312-Scientific editor work list.pdf
CrossCheck Report 80312-CrossCheck report.pdf