Publication Name	World Journal of Clinical Cases
Manuscript ID	69482
Country	China

Category	Pediatrics
Manuscript Type	Case Report
Article Title	Rare mutation in MKRN3 in two twin sisters with central precocious puberty: Two case reports
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
Funding Agency and Grant Number	Funding Agency Grant Number the key Research and Development Program of Zhejiang Province 2020C03121
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.
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

Received	2021-07-01 12:18
Peer-Review Started	2021-07-01 12:21
To Make the First Decision
Return for Revision	2021-07-16 02:38
Revised	2021-07-21 13:29
Second Decision	2021-09-09 03:19
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2021-09-10 09:16
Articles in Press	2021-09-10 09:16
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2021-10-29 01:37

ISSN	2307-8960 (online)
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