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Articles Published Processes
8/5/2021 2:37:05 PM | Browse: 594 | Download: 1613
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Received |
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2021-01-07 02:59 |
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Peer-Review Started |
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2021-01-07 03:00 |
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First Decision by Editorial Office Director |
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2021-02-12 01:06 |
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Return for Revision |
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2021-02-12 01:06 |
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Revised |
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2021-03-04 08:12 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2021-06-28 12:43 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2021-06-28 12:48 |
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Articles in Press |
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2021-06-28 12:48 |
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Edit the Manuscript by Language Editor |
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2021-07-04 02:52 |
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Typeset the Manuscript |
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2021-07-28 05:45 |
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Publish the Manuscript Online |
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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/ |
| 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 |
Geriatrics & Gerontology |
| Manuscript Type |
Case Report |
| Article Title |
2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report
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| 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 |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| The Fundamental Research Funds of Health Commission of Sichuan Province |
17ZD035 |
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| Corresponding Author |
Xue-Yan Wang, MD, N/A, 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 |
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