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Articles Published Processes
3/30/2023 1:19:28 PM | Browse: 363 | Download: 1429
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Received |
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2022-12-02 11:03 |
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Peer-Review Started |
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2022-12-02 11:04 |
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First Decision by Editorial Office Director |
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2023-01-17 01:23 |
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Return for Revision |
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2023-01-17 01:23 |
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Revised |
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2023-01-30 11:01 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2023-03-15 02:58 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2023-03-15 08:39 |
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Articles in Press |
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2023-03-15 08:39 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2023-03-17 11:59 |
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Publish the Manuscript Online |
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2023-03-30 13:19 |
| 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: https://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 |
Endocrinology & Metabolism |
| Manuscript Type |
Case Report |
| Article Title |
Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Ning Yuan, Lin Lu, Xiao-Ping Xing, Ou Wang, Yue Jiang, Ji Wu, Ming-Hai He, Xiao-Juan Wang and Le-Wei Cao |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| National Natural Science Foundation of China |
82070817 |
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| Corresponding Author |
Lin Lu, MD, Professor, Department of Endocrinology, Key Laboratory of National health commission, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Science, No. 1 Shuaifuyuan, Wangfujing, Dongcheng District, Beijing 100730, China. lulin88@sina.com |
| Key Words |
Hypocalcemia; Hypomagnesemia; Hypoparathyroidism; Kenny-Caffey syndrome type 2; FAM111A gene; Case report |
| Core Tip |
The FAM111A mutation was more likely to be a de novo mutation. Since the patient was an adult at the time of consultation, long-term follow-up treatment and observation of electrolyte status is necessary. Moreover, the fertility of the patient and the genetics of her offspring should be determined. |
| Publish Date |
2023-03-30 13:19 |
| Citation |
Yuan N, Lu L, Xing XP, Wang O, Jiang Y, Wu J, He MH, Wang XJ, Cao LW. Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report. World J Clin Cases 2023; 11(10): 2290-2300 |
| URL |
https://www.wjgnet.com/2307-8960/full/v11/i10/2290.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v11.i10.2290 |
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