Publication Name	World Journal of Cardiology
Manuscript ID	87708
Country	China

Received	2023-08-23 14:29
Peer-Review Started	2023-08-23 14:32
First Decision by Editorial Office Director	2023-10-09 07:06
Return for Revision	2023-10-09 07:06
Revised	2023-10-19 14:06
Publication Fee Transferred
Second Decision by Editor	2023-10-30 02:05
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director	2023-11-03 08:05
Articles in Press	2023-11-03 08:05
Edit the Manuscript by Language Editor
Typeset the Manuscript	2023-11-20 06:39
Publish the Manuscript Online	2023-11-23 08:41

ISSN	1949-8462 (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	Cardiac & Cardiovascular Systems
Manuscript Type	Case Report
Article Title	Hypertrophic cardiomyopathy secondary to deficiency in lysosome-associated membrane protein-2: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Ye-Tong Zhao, Xiu-Qun Cao and Xiao-Lin Mu
Funding Agency and Grant Number
Corresponding Author	Xiao-Lin Mu, MA, Doctor, Doctor, Department of Radiology, Central Hospital of Dalian University of Technology, No. 826 Southwest Road, Shahekou District, Dalian 116033, Liaoning Province, China. dugumuxin@163.com
Key Words	Danon disease; Lysosome-associated membrane protein-2 gene; Cardiomyopathy; Hypertrophy; Cardiac magnetic resonance imaging; Myocardial strain; Case report
Core Tip	Danon disease (DD) is a rare X-linked disorder caused by a deficiency of lysosome-associated membrane protein-2. DD is clinically characterized by severe cardiomyopathy, skeletal muscle disease, and intellectual disability. The most frequent high-risk form of DD is cardiomyopathy, which can result in arrhythmia(s), early-onset heart failure, and even sudden cardiac death. The intent of our case report is to raise the awareness of DD, and to improve the clinical suspicion of DD.
Publish Date	2023-11-23 08:41
Citation	Zhao YT, Cao XQ, Mu XL. Hypertrophic cardiomyopathy secondary to deficiency in lysosome-associated membrane protein-2: A case report. World J Cardiol 2023; 15(11): 609-614
URL	https://www.wjgnet.com/1949-8462/full/v15/i11/609.htm
DOI	https://dx.doi.org/10.4330/wjc.v15.i11.609

Full Article (PDF)	WJC-15-609-with-cover.pdf
Full Article (Word)	WJC-15-609.docx
CARE Checklist–2016	87708-CARE Checklist (2016).pdf
Manuscript File	87708_Auto_Edited-LJH-JLW.docx
Answering Reviewers	87708-Answering reviewers.pdf
Audio Core Tip	87708-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	87708-Conflict-of-interest statement.pdf
Copyright License Agreement	87708-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s)	87708-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	87708-Language certificate.pdf
Peer-review Report	87708-Peer-review(s).pdf
Journal Editor-in-Chief Review Report	87708-Journal editor-in-chief review report.pdf
Scientific Misconduct Check	87708-Bing-Liu JH-2.png
Scientific Misconduct Check	87708-CrossCheck.png
Scientific Editor Work List	87708-Scientific editor work list.pdf
CrossCheck Report	87708-CrossCheck report.pdf