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Articles Published Processes
2/24/2023 9:09:48 AM | Browse: 257 | Download: 792
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Received |
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2022-10-05 02:29 |
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Peer-Review Started |
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2022-10-05 02:30 |
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First Decision by Editorial Office Director |
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2022-11-22 00:42 |
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Return for Revision |
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2022-11-22 00:42 |
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Revised |
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2022-12-17 03:49 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2023-01-10 03:21 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2023-01-10 10:28 |
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Articles in Press |
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2023-01-10 10:28 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2023-01-12 07:30 |
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Publish the Manuscript Online |
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2023-02-24 09:09 |
| 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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| 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 |
Clinical manifestations of adult hereditary spherocytosis with novel SPTB gene mutations and hyperjaundice: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Ni Jiang, Wu-Yong Mao, Bing-Xue Peng, Ting-Ya Yang and Xiao-Rong Mao |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| Natural Science Foundation of Gansu Province |
21JR1RA070 |
| Construction of Clinical Medical Research Center |
21JR7RA392 |
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| Corresponding Author |
Xiao-Rong Mao, MD, Chief Physician, Department of Infectious Diseases, The First Hospital of Lanzhou University, No. 1 Donggang West Road, Chengguan District, Lanzhou 730000, Gansu Province, China. mxr2013@126.com |
| Key Words |
Gall-stone; Jaundice; Hereditary spherocytosis; Gene mutations; Adult; Case report |
| Core Tip |
A novel mutation in the SPTB gene was identified in a patient with hemolytic anemia, which caused the patient to present with extremely high jaundice without obvious hemolysis. At the same time, there was no similar mutation in the patient’s family. Because medical treatment was ineffective, we finally performed splenectomy after communicating with the patient. After splenectomy, the patient’s liver function recovered. The patient’s liver function continued to be normal during follow-up. |
| Publish Date |
2023-02-24 09:09 |
| Citation |
Jiang N, Mao WY, Peng BX, Yang TY, Mao XR. Clinical manifestations of adult hereditary spherocytosis with novel SPTB gene mutations and hyperjaundice: A case report. World J Clin Cases 2023; 11(6): 1349-1355 |
| URL |
https://www.wjgnet.com/2307-8960/full/v11/i6/1349.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v11.i6.1349 |
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