Publication Name	World Journal of Clinical Cases
Manuscript ID	87260
Country	China

Received	2023-08-01 16:10
Peer-Review Started	2023-08-01 16:13
To Make the First Decision
Return for Revision	2023-08-30 07:13
Revised	2023-10-21 14:22
Second Decision	2023-11-02 03:03
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2023-11-02 08:36
Articles in Press	2023-11-02 08:36
Publication Fee Transferred
Edit the Manuscript by Language Editor	2023-11-01 11:30
Typeset the Manuscript	2023-11-10 03:56
Publish the Manuscript Online	2023-11-16 04:01

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	Pediatrics
Manuscript Type	Case Report
Article Title	Type II Abernethy malformation with cystic fibrosis in a 12-year-old girl: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Li-Jie Zhang, Xing-Yu Liu, Teng-Fei Chen, Zhong-Ya Xu and Han-Jun Yin
ORCID	Author(s) ORCID Number Han-Jun Yin http://orcid.org/0000-0002-4618-7945
Funding Agency and Grant Number
Corresponding Author	Han-Jun Yin, MD, Attending Doctor, Department of Pediatrics, Nanjing Drum Tower Hospital Group Suqian Hospital, No. 138 South Huanghe Road, Suqian 223800, Jiangsu Province, China. jssqyhj@163.com
Key Words	Abernethy malformation; Cystic fibrosis; CFTR gene; Case report
Core Tip	Abernethy malformation, also referred to as congenital extrahepatic portosystemic shunt, is an uncommon malformation resulting from anomalous development of the portal venous system. Cystic fibrosis (CF) is an autosomal recessive disorder caused by mutations in the CFTR gene, which is rare in Asian populations. We present an Asian child with type II Abernethy malformation coexisting with CF and discuss the diagnosis and treatment of Abernethy malformation and CF.
Publish Date	2023-11-16 04:01
Citation	Zhang LJ, Liu XY, Chen TF, Xu ZY, Yin HJ. Type II Abernethy malformation with cystic fibrosis in a 12-year-old girl: A case report. World J Clin Cases 2023; 11(32): 7865-7871
URL	https://www.wjgnet.com/2307-8960/full/v11/i32/7865.htm
DOI	https://dx.doi.org/10.12998/wjcc.v11.i32.7865

Full Article (PDF)	WJCC-11-7865-with-cover.pdf
Full Article (Word)	WJCC-11-7865.docx
CARE Checklist–2016	87260-CARE Checklist (2016).pdf
Manuscript File	87260_Auto_Edited-LJH-Webster J-JLW.docx
Answering Reviewers	87260-Answering reviewers.pdf
Audio Core Tip	87260-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	87260-Conflict-of-interest statement.pdf
Copyright License Agreement	87260-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	87260-Grant application form(s).pdf
Signed Consent for Treatment Form(s) or Document(s)	87260-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	87260-Language certificate.pdf
Peer-review Report	87260-Peer-review(s).pdf
Scientific Misconduct Check	87260-Bing-Liu JH-2.png
Scientific Misconduct Check	87260-CrossCheck.png
Scientific Editor Work List	87260-Scientific editor work list.pdf