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Articles Published Processes
10/30/2024 10:50:20 AM | Browse: 135 | Download: 736
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Received |
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2024-06-26 14:42 |
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Peer-Review Started |
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2024-06-26 14:42 |
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First Decision by Editorial Office Director |
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2024-09-17 02:56 |
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Return for Revision |
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2024-09-18 03:35 |
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Revised |
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2024-09-25 18:41 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2024-10-14 02:40 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2024-10-15 03:31 |
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Articles in Press |
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2024-10-15 03:31 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2024-10-28 03:21 |
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Publish the Manuscript Online |
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2024-10-30 10:50 |
| ISSN |
2219-2808 (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: https://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2024. 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 |
Genetics & Heredity |
| Manuscript Type |
Retrospective Cohort Study |
| Article Title |
Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Jin-Ying You, Ling-Yun Xiong, Min-Fang Wu, Jun-Song Fan, Qi-Hua Fu and Ming-Hua Qiu |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| The Xiamen Municipal Science and Technology Bureau Project |
No. 3502Z20209177 |
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| Corresponding Author |
Jin-Ying You, Chief Physician, Department of Neonatal, The Second Affiliated Hospital of Xiamen Medical College, No. 566 Shengguang Road, Jiemei District, Xiamen 361021, Fujian Province, China. youjafb@163.com |
| Key Words |
Hyperbilirubinemia; Gene mutation; Neonates; Genetic polymorphisms; Inherited diseases |
| Core Tip |
Variations in the frequency and distribution of gene mutations are observed in neonatal hyperbilirubinemia (NH) caused by inherited diseases, with uridine 5'-diphospho-glucuronosyltransferase 1A1 mutations prevalent in neonatal Gilbert syndrome cases, Na+/taurocholate cotransporting polypeptide Ntcp mutations in sodium taurocholate cotransporting polypeptide deficiency patients, and Adenosine triphosphatase mutations in Wilson's disease. The distinct genetic profiles between the high-risk and low-risk groups suggest the potential utility of genetic screening for risk stratification and early intervention in NH. |
| Publish Date |
2024-10-30 10:50 |
| Citation |
You JY, Xiong LY, Wu MF, Fan JS, Fu QH, Qiu MH. Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases. World J Clin Pediatr 2024; 13(4): 98462 |
| URL |
https://www.wjgnet.com/2219-2808/full/v13/i4/98462.htm |
| DOI |
https://dx.doi.org/10.5409/wjcp.v13.i4.98462 |
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