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Articles Published Processes
9/10/2021 7:23:16 AM | Browse: 363 | Download: 1102
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Received |
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2021-04-22 08:48 |
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Peer-Review Started |
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2021-04-22 08:49 |
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To Make the First Decision |
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Return for Revision |
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2021-05-24 01:36 |
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Revised |
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2021-05-27 13:15 |
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Second Decision |
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2021-07-19 03:12 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-07-19 06:01 |
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Articles in Press |
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2021-07-19 06:01 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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2021-07-28 02:05 |
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Typeset the Manuscript |
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2021-09-01 08:23 |
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Publish the Manuscript Online |
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2021-09-10 07:23 |
| 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) 2021. 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 |
Case Report |
| Article Title |
Diagnosis and treatment of an inborn error of bile acid synthesis type 4: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Shou-Hao Wang, Tian-Chen Hui, Zhe-Wen Zhou, Cheng-An Xu, Wen-Hao Wu, Qing-Qing Wu, Wei Zheng, Qiao-Qiao Yin and Hong-Ying Pan |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Hong-Ying Pan, MM, Professor, Qingdao Medical College, Qingdao University, No. 1 Ningde Road, Qingdao 266073, Shandong Province, China. hypanzjsrmyy@126.com |
| Key Words |
Bile acid synthesis; A-methylacyl-CoA racemase gene; Gene mutation; Inborn error of metabolism; Ursodeoxycholic acid; Case report |
| Core Tip |
Inborn error of bile acid synthesis type 4 is a peroxisomal disease with impaired bile acid synthesis caused by a-methylacyl-CoA racemase gene mutation. This is the first report of an adult patient with liver disease and fat-soluble vitamin deficiency. The patient had significantly improved prognosis after treatment. In adult patients with recurrent liver function abnormalities, physicians should be alert to the possibility of genetic disorders, which can be diagnosed by genetic testing or, if possible, combined with mass spectrometry. |
| Publish Date |
2021-09-10 07:23 |
| Citation |
Wang SH, Hui TC, Zhou ZW, Xu CA, Wu WH, Wu QQ, Zheng W, Yin QQ, Pan HY. Diagnosis and treatment of an inborn error of bile acid synthesis type 4: A case report. World J Clin Cases 2021; 9(26): 7923-7929 |
| URL |
https://www.wjgnet.com/2307-8960/full/v9/i26/7923.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v9.i26.7923 |
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