Publication Name	World Journal of Clinical Cases
Manuscript ID	52469
Country	China

Received	2019-11-13 13:11
Peer-Review Started	2019-11-13 13:15
To Make the First Decision
Return for Revision	2020-02-20 23:34
Revised	2020-02-27 03:02
Second Decision	2020-03-04 14:19
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-03-05 07:22
Articles in Press	2020-03-05 07:22
Publication Fee Transferred
Edit the Manuscript by Language Editor	2020-03-08 23:43
Typeset the Manuscript	2020-03-16 09:03
Publish the Manuscript Online	2020-03-26 03:19

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: http://creativecommons.org/licenses/by-nc/4.0/
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Category	Endocrinology & Metabolism
Manuscript Type	Case Report
Article Title	Growth hormone therapy for children with KBG syndrome: A case report and review of literature
Manuscript Source	Unsolicited Manuscript
All Author List	Xiu-Ying Ge, Long Ge, Wen-Wen Hu, Xiao-Ling Li and Yan-Yan Hu
ORCID	Author(s) ORCID Number Xiu-Ying Ge http://orcid.org/0000-0002-4939-1060 Long Ge http://orcid.org/0000-0001-5737-516X Wen-Wen Hu http://orcid.org/0000-0002-8228-8292 Xiao-Ling Li http://orcid.org/0000-0001-8907-7394 Yan-Yan Hu http://orcid.org/0000-0001-6444-8961
Funding Agency and Grant Number
Corresponding Author	Yan-Yan Hu, MD, Department of Pediatrics, Linyi People’s Hospital, No. 27, Eastern Jiefang Road, Linyi 276000, Shandong Province, China. hyanyansmile@hotmail.com
Key Words	Growth hormone therapy; KBG syndrome; ANKRD11 gene; Short stature; Children; Case report
Core Tip	KBG syndrome is a rare autosomal dominant disorder. The percentage of height below 10th centile was 66%. It is relatively high. Children with KBG syndrome accompanied by short stature could benefit from growth hormone therapy.
Publish Date	2020-03-26 03:19
Citation	Ge XY, Ge L, Hu WW, Li XL, Hu YY. Growth hormone therapy for children with KBG syndrome: A case report and review of literature. World J Clin Cases 2020; 8(6): 1172-1179
URL	https://www.wjgnet.com/2307-8960/full/v8/i6/1172.htm
DOI	https://dx.doi.org/10.12998/wjcc.v8.i6.1172

Full Article (PDF)	WJCC-8-1172.pdf
Full Article (Word)	WJCC-8-1172.docx
Manuscript File	52469-Review_WangTQ.doc
Answering Reviewers	52469-Answering reviewers.pdf
Audio Core Tip	52469-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	52469-Conflict-of-interest statement.pdf
Copyright License Agreement	52469-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	52469-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	52469-Language certificate.pdf
Peer-review Report	52469-Peer-review(s).pdf
Scientific Misconduct Check	52469-Scientific misconduct check.pdf
Scientific Editor Work List	52469-Scientific editor work list.pdf