BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
12/2/2022 12:50:19 PM | Browse: 241 | Download: 749
Publication Name World Journal of Clinical Cases
Manuscript ID 79911
Country China
Received
2022-09-11 16:27
Peer-Review Started
2022-09-11 16:28
To Make the First Decision
Return for Revision
2022-10-13 01:23
Revised
2022-10-20 08:33
Second Decision
2022-11-04 03:39
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2022-11-04 08:49
Articles in Press
2022-11-04 08:49
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2022-11-14 12:50
Publish the Manuscript Online
2022-12-02 12:50
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) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Andrology
Manuscript Type Case Report
Article Title Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report
Manuscript Source Unsolicited Manuscript
All Author List Tian-Qin Deng, Yu-Li Xie, Jiang-Bo Pu, Jiang Xuan and Xue-Mei Li
ORCID
Author(s) ORCID Number
Tian-Qin Deng http://orcid.org/0000-0002-1994-0794
Funding Agency and Grant Number
Corresponding Author Tian-Qin Deng, PhD, Chief Doctor, Reproductive Medical Center, Affiliated Shenzhen Maternity & Child Healthcare Hospital, Southern Medical University, No. 3012 Fuqiang Road, Shenzhen 518028, Guangdong Province, China. tianqin02@163.com
Key Words Acephalic spermatozoa syndrome; PMFBPI; Infertility; Male; Sperm; Case report
Core Tip Acephalic spermatozoa syndrome (ASS) is an extremely rare form of teratozoospermia. Patients with ASS are often unable to conceive naturally, and intracytoplasmic sperm injection is the main method used for such patients to produce biological offspring. Recent studies have shown that ASS is associated with inherited genetic mutations.
Publish Date 2022-12-02 12:50
Citation Deng TQ, Xie YL, Pu JB, Xuan J, Li XM. Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report. World J Clin Cases 2022; 10(34):12761-12767
URL https://www.wjgnet.com/2307-8960/full/v10/i34/12761.htm
DOI https://dx.doi.org/10.12998/wjcc.v10.i34.12761
Full Article (PDF) WJCC-10-12761.pdf
Full Article (Word) WJCC-10-12761.docx
CARE Checklist–2016 79911-CARE-Checklist–2016-revision.docx
Manuscript File 79911_Auto_Edited-LJH-JLW.docx
Answering Reviewers 79911-Answering reviewers.pdf
Audio Core Tip 79911-Audio core tip.m4a
Conflict-of-Interest Disclosure Form 79911-Conflict-of-interest statement.pdf
Copyright License Agreement 79911-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s) 79911-Grant application form(s).pdf
Signed Consent for Treatment Form(s) or Document(s) 79911-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate 79911-Language certificate.pdf
Peer-review Report 79911-Peer-review(s).pdf
Scientific Misconduct Check 79911-Bing-Liu JH-2.jpg
Scientific Misconduct Check 79911-CrossCheck.jpg
Scientific Editor Work List 79911-Scientific editor work list.pdf