Publication Name	World Journal of Clinical Cases
Manuscript ID	54622
Country	China

Received	2020-02-10 14:08
Peer-Review Started	2020-02-10 14:08
To Make the First Decision
Return for Revision	2020-03-05 23:15
Revised	2020-03-26 09:11
Second Decision	2020-04-16 09:38
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-04-16 22:49
Articles in Press	2020-04-16 22:49
Publication Fee Transferred
Edit the Manuscript by Language Editor	2020-04-25 02:07
Typeset the Manuscript	2020-05-15 11:13
Publish the Manuscript Online	2020-05-25 09:57

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	Gastroenterology & Hepatology
Manuscript Type	Case Report
Article Title	Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports
Manuscript Source	Unsolicited Manuscript
All Author List	Ling-Ling Kang, Ze-Lin Liu and Hou-De Zhang
ORCID	Author(s) ORCID Number Ling-Ling Kang http://orcid.org/0000-0003-1669-3617 Ze-Lin Liu http://orcid.org/0000-0002-3720-9380 Hou-De Zhang http://orcid.org/0000-0001-8680-0073
Funding Agency and Grant Number
Corresponding Author	Hou-De Zhang, MD, Professor, Department of Gastroenterology, Nanshan Hospital, Guangdong Medical University, 89 Taoyuan Road, Nanshan District, Shenzhen 518052, Guangdong Province, China. szkjk@126.com
Key Words	Gilbert’s syndrome; Hereditary spherocytosis; Unconjugated hyperbilirubinemia; Erythrocyte lifespan; Levitt’s CO breath test; Case report
Core Tip	The coexistence of Gilbert’s syndrome with a hemolytic disease can impede diagnosis. Gilbert’s syndrome-hemolysis disease comorbidity should be suspected in patients who present with isolated unconjugated hyperbilirubinemia when serum bilirubin levels are discordant with hemoglobin levels, especially if there are even subtle signs of possible hemolysis. Levitt’s CO breath test for erythrocyte lifespan determination and broadly available genetic tests can be used for rapid diagnosis of these conditions.
Publish Date	2020-05-25 09:57
Citation	Kang LL, Liu ZL, Zhang HD. Gilbert’s syndrome coexisting with hereditary spherocytosis might not be rare: Six case reports. World J Clin Cases 2020; 8(10): 2001-2008
URL	https://www.wjgnet.com/2307-8960/full/v8/i10/2001.htm
DOI	https://dx.doi.org/10.12998/wjcc.v8.i10.2001

Full Article (PDF)	WJCC-8-2001.pdf
Full Article (Word)	WJCC-8-2001.docx
CARE Checklist–2016	54622-CARE-Checklist–2016-revision.pdf
Manuscript File	54622-Review-Filipodia.doc
Answering Reviewers	54622-Answering reviewers.pdf
Audio Core Tip	54622-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	54622-Conflict-of-interest statement.pdf
Copyright License Agreement	54622-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	54622-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	54622-Language certificate.pdf
Peer-review Report	54622-Peer-review(s).pdf
Scientific Misconduct Check	54622-Scientific misconduct check.pdf
Scientific Editor Work List	54622-Scientific editor work list.pdf