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1/26/2023 5:44:49 PM | Browse: 97 | Download: 228
Publication Name World Journal of Clinical Cases
Manuscript ID 78857
Country/Territory China
Received
2022-07-18 12:57
Peer-Review Started
2022-07-18 13:00
To Make the First Decision
Return for Revision
2022-10-17 07:58
Revised
2022-10-21 12:48
Second Decision
2022-12-08 03:14
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2022-12-09 00:34
Articles in Press
2022-12-09 00:34
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2022-12-19 05:55
Publish the Manuscript Online
2023-01-26 17:44
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) 2023. 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 Gastroenterology & Hepatology
Manuscript Type Case Report
Article Title Congenital biliary atresia caused by GPC1 gene mutation in Chinese siblings: A case report
Manuscript Source Unsolicited Manuscript
All Author List Yuan-Mei Kong, Ke Yuan and Chun-Lin Wang
ORCID
Author(s) ORCID Number
Yuan-Mei Kong http://orcid.org/0000-0002-3250-1892
Ke Yuan http://orcid.org/0000-0002-0458-3683
Chun-Lin Wang http://orcid.org/0000-0002-4273-1341
Funding Agency and Grant Number
Corresponding Author Chun-Lin Wang, MD, PhD, Chief Doctor, Department of Pediatrics, The First Affiliated Hospital of Zhejiang University, No. 79 Qingchun Road, Hangzhou 310003, Zhejiang Province, China. hzwangcl@zju.edu.cn
Key Words Congenital biliary atresia; Jaundice; Etiology; GPC1; Liver transplantation; Case report
Core Tip Congenital biliary atresia (CBA) often results in a poor prognosis. Most patients need liver transplantation as the final treatment. If the opportunity for liver transplantation is missed, death often occurs. However, the etiology of CBA is still unclear. Clarifying the etiology is of great significance for prognosis, treatment, and genetic counseling. Through the report of a patient with a GPC1 mutation, this paper enriches the genetic etiology of CBA and provides a new basis for clinical and scientific research.
Publish Date 2023-01-26 17:44
Citation Kong YM, Yuan K, Wang CL. Congenital biliary atresia caused by GPC1 gene mutation in Chinese siblings: A case report. World J Clin Cases 2023; 11(3): 629-634
URL https://www.wjgnet.com/2307-8960/full/v11/i3/629.htm
DOI https://dx.doi.org/10.12998/wjcc.v11.i3.629
Full Article (PDF) WJCC-11-629.pdf
Full Article (Word) WJCC-11-629.docx
Manuscript File 78857_Auto_Edited-LJH-JLW.docx
Answering Reviewers 78857-Answering reviewers.pdf
Audio Core Tip 78857-Audio core tip.m4a
Conflict-of-Interest Disclosure Form 78857-Conflict-of-interest statement.pdf
Copyright License Agreement 78857-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s) 78857-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate 78857-Language certificate.pdf
Peer-review Report 78857-Peer-review(s).pdf
Scientific Misconduct Check 78857-Bing-Liu JH-2.jpg
Scientific Misconduct Check 78857-CrossCheck.jpg
Scientific Editor Work List 78857-Scientific editor work list.pdf