Publication Name	World Journal of Clinical Cases
Manuscript ID	62346
Country	China

Received	2021-01-07 02:59
Peer-Review Started	2021-01-07 03:00
To Make the First Decision
Return for Revision	2021-02-12 01:06
Revised	2021-03-04 08:12
Second Decision	2021-06-28 12:43
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2021-06-28 12:48
Articles in Press	2021-06-28 12:48
Publication Fee Transferred
Edit the Manuscript by Language Editor	2021-07-04 02:52
Typeset the Manuscript	2021-07-28 05:45
Publish the Manuscript Online	2021-08-05 14:37

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	Geriatrics & Gerontology
Manuscript Type	Case Report
Article Title	2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Na Xi, Xiao Song, Xue-Yan Wang, Sheng-Fang Qin, Guan-Nan He, Ling-Ling Sun and Xi-Min Chen
ORCID	Author(s) ORCID Number Na Xi http://orcid.org/0000-0003-1159-2008 Xiao Song http://orcid.org/0000-0001-8914-3881 Xue-Yan Wang http://orcid.org/0000-0003-0486-6867 Sheng-Fang Qin http://orcid.org/0000-0001-9391-890X Guan-Nan He http://orcid.org/0000-0003-0131-1268 Ling-Ling Sun http://orcid.org/0000-0002-7169-4009 Xi-Min Chen http://orcid.org/0000-0001-6644-3689
Funding Agency and Grant Number	Funding Agency Grant Number The Fundamental Research Funds of Health Commission of Sichuan Province 17ZD035
Corresponding Author	Xue-Yan Wang, MD, N/A, Department of Medical Genetics and Prenatal Diagnosis, Sichuan Provincial Hospital for Women and Children, No. 290 Shayanxi Er Street, Wuhou District, Chengdu 610045, Sichuan Province, China. wang_xueyan20@21cn.com
Key Words	CYP21A2 gene mutations; Congenital adrenal hyperplasia; Pregnancy; Genetic counseling; Genetic testing; Pathogenic point mutations; Alleles
Core Tip	This study suggests that carriers of type 2+0 are likely to be a trap in genetic testing and genetic counseling.
Publish Date	2021-08-05 14:37
Citation	Xi N, Song X, Wang XY, Qin SF, He GN, Sun LL, Chen XM. 2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report. World J Clin Cases 2021; 9(23): 6789-6797
URL	https://www.wjgnet.com/2307-8960/full/v9/i23/6789.htm
DOI	https://dx.doi.org/10.12998/wjcc.v9.i23.6789

Full Article (PDF)	WJCC-9-6789.pdf
Full Article (Word)	WJCC-9-6789.docx
Manuscript File	62346_Review-FilipodiaCL.docx
Answering Reviewers	62346-Answering reviewers.pdf
Audio Core Tip	62346-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	62346-Conflict-of-interest statement.pdf
Copyright License Agreement	62346-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	62346-Grant application form(s).pdf
Signed Informed Consent Form(s) or Document(s)	62346-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	62346-Language certificate.pdf
Peer-review Report	62346-Peer-review(s).pdf
Scientific Misconduct Check	62346-Scientific misconduct check.pdf
Scientific Editor Work List	62346-Scientific editor work list.pdf