Publication Name	World Journal of Clinical Cases
Manuscript ID	77317
Country	China

Received	2022-04-24 22:17
Peer-Review Started	2022-04-24 22:19
To Make the First Decision
Return for Revision	2022-05-12 07:32
Revised	2022-05-25 13:59
Second Decision	2022-07-18 03:01
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2022-07-22 01:58
Articles in Press	2022-07-22 01:58
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2022-08-16 00:59
Publish the Manuscript Online	2022-08-26 09:54

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	Respiratory System
Manuscript Type	Case Report
Article Title	CCNO mutation as a cause of primary ciliary dyskinesia: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Yun-Yan Zhang, Yan Lou, Yan Han and Hao Tang
ORCID	Author(s) ORCID Number Yun-Yan Zhang http://orcid.org/0000-0002-6873-0443 Yan Lou http://orcid.org/0000-0002-5998-7917 Yan Han http://orcid.org/0000-0003-3849-2998 Hao Tang http://orcid.org/0000-0003-1536-1944
Funding Agency and Grant Number
Corresponding Author	Hao Tang, MD, PhD, Chief Doctor, Department of Respiratory and Critical Care Medicine, Changzheng Hospital, Naval Military Medical University, No. 415 Fengyang Road, Shanghai 200003, China. tanghao_0921@126.com
Key Words	Primary ciliary immobility disorder; CCNO gene; Whole exon gene sequencing; Clinical profiles; Review of literature; Case report
Core Tip	Primary ciliary dyskinesia (PCD) is a disease that is genetically diverse. Despite the discovery of more than 40 pathogenic genes, there are still insufficient case reports to help clinical diagnosis and treatment. We describe a case of primary ciliary immobility dysfunction caused by mutations in the CCNO (encoding cyclin O) gene. The patient lacked the classic PCD triad and was readily overlooked. We require further genetic research and particular case reports.
Publish Date	2022-08-26 09:54
Citation	Zhang YY, Lou Y, Han Y, Tang H. CCNO mutation as a cause of primary ciliary dyskinesia: A case report. World J Clin Cases 2022; 10(25): 9148-9155
URL	https://www.wjgnet.com/2307-8960/full/v10/i25/9148.htm
DOI	https://dx.doi.org/10.12998/wjcc.v10.i25.9148

Full Article (PDF)	WJCC-10-9148.pdf
Full Article (Word)	WJCC-10-9148.docx
CARE Checklist–2016	77317-CARE-Checklist–2016-revision_1152.pdf
Manuscript File	77317_Auto_Edited-LS.docx
Answering Reviewers	77317-Answering reviewers.pdf
Audio Core Tip	77317-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	77317-Conflict-of-interest statement.pdf
Copyright License Agreement	77317-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	77317-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	77317-Language certificate.pdf
Peer-review Report	77317-Peer-review(s).pdf
Scientific Misconduct Check	77317-Bing-Yan JP-2.png
Scientific Editor Work List	77317-Scientific editor work list.pdf
CrossCheck Report	77317-CrossCheck report.pdf