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Articles Published Processes
11/10/2021 1:44:24 AM | Browse: 381 | Download: 1092
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Received |
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2021-07-01 12:18 |
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Peer-Review Started |
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2021-07-01 12:21 |
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To Make the First Decision |
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Return for Revision |
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2021-07-16 02:38 |
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Revised |
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2021-07-21 13:29 |
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Second Decision |
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2021-09-09 03:19 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-09-10 09:16 |
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Articles in Press |
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2021-09-10 09:16 |
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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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2021-10-29 01:37 |
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Publish the Manuscript Online |
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2021-11-10 01:44 |
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 |
Pediatrics |
Manuscript Type |
Case Report |
Article Title |
Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Li-Qiong Jiang, Yan-Qiong Zhou, Ke Yuan, Jian-Fang Zhu, Yan-Lan Fang and Chun-Lin Wang |
ORCID |
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Funding Agency and Grant Number |
Funding Agency |
Grant Number |
the key Research and Development Program of Zhejiang Province |
2020C03121 |
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Corresponding Author |
Chun-Lin Wang, MD, PhD, Chief Doctor, Department of Pediatrics, The First Affiliated Hospital, Zhejiang University School of Medicine, No. 79 Qingchun Road, Hangzhou 310003, Zhejiang Province, China. hzwangcl@zju.edu.cn |
Key Words |
Central precocious puberty; MKRN3; Mutation; Case report |
Core Tip |
This report discusses the diagnosis and treatment of central precocious puberty caused by a new Makorin ring finger protein 3 gene mutation and includes a detailed clinical and laboratory analysis of the pathogenic principle, which provided the diagnosis and led to the treatment of central precocious puberty. |
Publish Date |
2021-11-10 01:44 |
Citation |
Jiang LQ, Zhou YQ, Yuan K, Zhu JF, Fang YL, Wang CL. Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports. World J Clin Cases 2021; 9(32): 10018-10023 |
URL |
https://www.wjgnet.com/2307-8960/full/v9/i32/10018.htm |
DOI |
https://dx.doi.org/10.12998/wjcc.v9.i32.10018 |
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