Publication Name	World Journal of Clinical Cases
Manuscript ID	62079
Country	China

Received	2020-12-30 06:19
Peer-Review Started	2020-12-30 06:20
To Make the First Decision
Return for Revision	2021-01-10 19:15
Revised	2021-01-21 16:46
Second Decision	2021-02-08 04:34
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2021-02-08 18:50
Articles in Press	2021-02-08 18:50
Publication Fee Transferred
Edit the Manuscript by Language Editor	2021-02-26 11:08
Typeset the Manuscript	2021-04-19 22:32
Publish the Manuscript Online	2021-04-22 12:14

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	Endocrinology & Metabolism
Manuscript Type	Case Report
Article Title	Alström syndrome with a novel mutation of ALMS1 and Graves’ hyperthyroidism: A case report and review of literature
Manuscript Source	Unsolicited Manuscript
All Author List	Juan-Juan Zhang, Jun-Qi Wang, Man-Qing Sun, De Xu, Yuan Xiao, Wen-Li Lu and Zhi-Ya Dong
ORCID	Author(s) ORCID Number Juan-Juan Zhang http://orcid.org/0000-0002-9349-1026 Jun-Qi Wang http://orcid.org/0000-0002-3297-5158 Man-Qing Sun http://orcid.org/0000-0002-4500-5628 De Xu http://orcid.org/0000-0003-2560-2588 Yuan Xiao http://orcid.org/0000-0002-4927-8199 Wen-Li Lu http://orcid.org/0000-0002-5027-8372 Zhi-Ya Dong http://orcid.org/0000-0002-2436-7857
Funding Agency and Grant Number
Corresponding Author	Zhi-Ya Dong, MD, Chief Physician, Department of Pediatrics, Ruijin Hospital, Shanghai Jiao-Tong University, School of Medicine, Ruijin 2nd Road, Shanghai 200025, China. dzy831@126.com
Key Words	ALMS1; Alström syndrome; Stop-gain mutations; Protein truncation; Graves’ hyperthyroidism; Case report
Core Tip	We reported the case of an 8-year-old girl who carried two novel mutations in ALMS1 according to the gene panel and developed Graves’ hyperthyroidism 2 years later. As far as we know, this is the first case reporting the association between Alström syndrome and Graves’ hyperthyroidism.
Publish Date	2021-04-22 12:14
Citation	Zhang JJ, Wang JQ, Sun MQ, Xu D, Xiao Y, Lu WL, Dong ZY. Alström syndrome with a novel mutation of ALMS1 and Graves’ hyperthyroidism: A case report and review of literature. World J Clin Cases 2021; 9(13): 3200-3211
URL	https://www.wjgnet.com/2307-8960/full/v9/i13/3200.htm
DOI	https://dx.doi.org/10.12998/wjcc.v9.i13.3200

Full Article (PDF)	WJCC-9-3200.pdf
Full Article (Word)	WJCC-9-3200.docx
CARE Checklist–2016	62079-CARE-Checklist–2016-revision.pdf
Manuscript File	62079_Auto_Edited_LM-Webster J-Clear.docx
Answering Reviewers	62079-Answering reviewers.pdf
Audio Core Tip	62079-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	62079-Conflict-of-interest statement.pdf
Copyright License Agreement	62079-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	62079-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	62079-Language certificate.pdf
Peer-review Report	62079-Peer-review(s).pdf
Scientific Misconduct Check	62079-Scientific misconduct check.pdf
Scientific Editor Work List	62079-Scientific editor work list.pdf
CrossCheck Report	62079-CrossCheck report.pdf