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Articles Published Processes
1/21/2022 8:16:14 AM | Browse: 505 | Download: 1020
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Received |
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2021-05-22 10:48 |
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Peer-Review Started |
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2021-05-22 10:53 |
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To Make the First Decision |
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Return for Revision |
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2021-07-06 02:07 |
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Revised |
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2021-07-17 19:19 |
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Second Decision |
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2021-11-30 03:39 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-11-30 19:14 |
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Articles in Press |
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2021-11-30 19:14 |
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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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2022-01-18 04:32 |
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Publish the Manuscript Online |
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2022-01-21 08:16 |
ISSN |
1948-5182 (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 |
Gastroenterology & Hepatology |
Manuscript Type |
Review |
Article Title |
Recent updates on progressive familial intrahepatic cholestasis types 1, 2 and 3: Outcome and therapeutic strategies
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Manuscript Source |
Invited Manuscript |
All Author List |
Seema Alam and Bikrant Bihari Lal |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Seema Alam, MD, Professor, Department of Pediatric Hepatology, Institute of Liver and Biliary Sciences, D-1 Vasant Kunj, New Delhi 110070, India. seema_alam@hotmail.com |
Key Words |
Genotype; Biliary diversion; Gene therapy; Liver transplantation |
Core Tip |
The spectrum of clinical manifestations in progressive familial intrahepatic cholestasis varies from mild to severe leading to end stage liver disease necessitating liver transplantation. Medical therapy forms the mainstay of treatment of pruritus with surgical biliary diversion reserved for refractory cases. Apical sodium bile salt co-transporter inhibitors are among the most promising newer drugs. This article describes the recent advances in understanding the clinical course and emerging therapies. |
Publish Date |
2022-01-21 08:16 |
Citation |
Alam S, Lal BB. Recent updates on progressive familial intrahepatic cholestasis types 1, 2 and 3: Outcome and therapeutic strategies. World J Hepatol 2022; 14(1): 98-118 |
URL |
https://www.wjgnet.com/1948-5182/full/v14/i1/98.htm |
DOI |
https://dx.doi.org/10.4254/wjh.v14.i1.98 |
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