BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
1/26/2023 5:44:49 PM | Browse: 170 | Download: 589
 |
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 Executive 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
|
Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
|
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 |
|
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 |
© 2004-2025 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
California Corporate Number: 3537345