Publication Name	World Journal of Clinical Cases
Manuscript ID	85494
Country	China

Received	2023-06-06 17:59
Peer-Review Started	2023-06-06 18:00
To Make the First Decision
Return for Revision	2023-07-17 09:29
Revised	2023-07-31 12:47
Second Decision	2023-08-08 02:53
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2023-08-08 07:20
Articles in Press	2023-08-08 07:20
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2023-08-24 06:48
Publish the Manuscript Online	2023-09-01 09:10

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: https://creativecommons.org/Licenses/by-nc/4.0/
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Category	Urology & Nephrology
Manuscript Type	Case Report
Article Title	Novel COL4A3 synonymous mutation causes Alport syndrome coexistent with immunoglobulin A nephropathy in a woman: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Yu-Ting Chen, Wen-Ze Jiang and Ke-Da Lu
ORCID	Author(s) ORCID Number Yu-Ting Chen http://orcid.org/0000-0002-6771-0133 Wen-Ze Jiang http://orcid.org/0000-0003-1331-4036 Ke-Da Lu http://orcid.org/0000-0002-9934-3630
Funding Agency and Grant Number	Funding Agency Grant Number The Major Project of Zhejiang Administration of Traditional Chinese Medicine 2020ZZ008
Corresponding Author	Ke-Da Lu, MD, Doctor, Professor, Department of Nephrology, The Third Affiliated Hospital of Zhejiang Chinese Medical University, No. 219 Moganshan Road, Xihu District, Hangzhou 310005, Zhejiang Province, China. lukedaq@126.com
Key Words	Alport syndrome; Immunoglobulin A nephropathy; COL4A3 gene; Whole-exome sequencing; Renal biopsy; Case report
Core Tip	It is challenging to distinguish between Alport syndrome (AS) and immunoglobulin A (IgA) nephropathy solely based on clinical and pathological findings. This report highlights the diagnostic value of whole-exome sequencing in the precise diagnosis of AS and emphasizes the significance of renal biopsy and genetic detection in the early diagnosis of AS and familial IgA nephropathy.
Publish Date	2023-09-01 09:10
Citation	Chen YT, Jiang WZ, Lu KD. Novel COL4A3 synonymous mutation causes Alport syndrome coexistent with immunoglobulin A nephropathy in a woman: A case report. World J Clin Cases 2023; 11(25): 5947-5953
URL	https://www.wjgnet.com/2307-8960/full/v11/i25/5947.htm
DOI	https://dx.doi.org/10.12998/wjcc.v11.i25.5947

Full Article (PDF)	WJCC-11-5947-with-cover.pdf
Full Article (Word)	WJCC-11-5947.docx
CARE Checklist–2016	85494-CARE-Checklist–2016-revision.pdf
Manuscript File	85494_Auto_Edited-JLW.docx
Answering Reviewers	85494-Answering reviewers.pdf
Audio Core Tip	85494-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	85494-Conflict-of-interest statement.pdf
Copyright License Agreement	85494-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	85494-Grant application form(s).pdf
Signed Consent for Treatment Form(s) or Document(s)	85494-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	85494-Language certificate.pdf
Peer-review Report	85494-Peer-review(s).pdf
Scientific Misconduct Check	85494-Bing-Fan JR-2.png
Scientific Editor Work List	85494-Scientific editor work list.pdf