Publication Name	World Journal of Clinical Cases
Manuscript ID	70248
Country	China

Received	2021-07-27 14:04
Peer-Review Started	2021-07-27 14:06
To Make the First Decision
Return for Revision	2021-10-22 08:54
Revised	2021-11-02 01:35
Second Decision	2022-02-17 05:50
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2022-02-20 12:59
Articles in Press	2022-02-20 12:59
Publication Fee Transferred
Edit the Manuscript by Language Editor	2022-02-10 22:45
Typeset the Manuscript	2022-03-01 00:25
Publish the Manuscript Online	2022-03-22 14:35

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	Genetics & Heredity
Manuscript Type	Case Report
Article Title	Short stature associated with a novel mutation in the aggrecan gene: A case report and literature review
Manuscript Source	Unsolicited Manuscript
All Author List	Li-Ping Yin, Hong-Xue Zheng and Hong Zhu
ORCID	Author(s) ORCID Number Li-Ping Yin http://orcid.org/0000-0002-5965-037X Hong-Xue Zheng http://orcid.org/0000-0003-0929-6621 Hong Zhu http://orcid.org/0000-0001-5078-1288
Funding Agency and Grant Number
Corresponding Author	Hong Zhu, PhD, Professor, Department of Paediatrics, the First People’s Hospital of Changzhou, the Third Affiliated Hospital of Soochow University, Changzhou 213000, Jiangsu Province, China, Changzhou 213000, Jiangsu Province, China. zhuhongcz@126.com
Key Words	Short stature; Aggrecan gene; Mutation; Bone age; Case report
Core Tip	Because of the diversity of clinical manifestations, phenotype overlap, and high genetic heterogeneity of short stature, the etiology of dwarfism cannot be determined by merely inquiring about the medical history, clinical performances, and routine laboratory examination. Gene detection can provide clear clinical diagnostic evidence, decrease the medical error and missed diagnosis of the disorder, instruct genetic counseling, and supply a trustworthy principle for fetal diagnosis. This case expanded the spectrum of aggrecan gene mutations.
Publish Date	2022-03-22 14:35
Citation	Yin LP, Zheng HX, Zhu H. Short stature associated with a novel mutation in the aggrecan gene: A case report and literature review. World J Clin Cases 2022; 10(9): 2811-2817
URL	https://www.wjgnet.com/2307-8960/full/v10/i9/2811.htm
DOI	https://dx.doi.org/10.12998/wjcc.v10.i9.2811

Full Article (PDF)	WJCC-10-2811.pdf
Full Article (Word)	WJCC-10-2811.docx
CARE Checklist–2016	70248-CARE-Checklist–2016-revision.pdf
Manuscript File	70248_Auto_Edited-LJH-FilipodiadocxCL.docx
Answering Reviewers	70248-Answering reviewers.pdf
Audio Core Tip	70248-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	70248-Conflict-of-interest statement.pdf
Copyright License Agreement	70248-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	70248-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	70248-Language certificate.pdf
Peer-review Report	70248-Peer-review(s).pdf
Scientific Misconduct Check	70248-Bing-Liu JH-2.jpg
Scientific Misconduct Check	70248-CrossCheck.jpg
Scientific Editor Work List	70248-Scientific editor work list.pdf
CrossCheck Report	70248-CrossCheck report.pdf