Publication Name	World Journal of Hepatology
Manuscript ID	46996
Country	United States

Received	2019-03-11 06:14
Peer-Review Started	2019-03-12 09:26
To Make the First Decision	2019-04-04 01:15
Return for Revision	2019-04-10 08:20
Revised	2019-04-12 17:49
Second Decision	2019-04-19 07:45
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2019-04-19 20:35
Articles in Press	2019-04-19 20:35
Publication Fee Transferred
Edit the Manuscript by Language Editor	2019-04-25 13:58
Typeset the Manuscript	2019-05-25 07:09
Publish the Manuscript Online	2019-05-27 08:24

ISSN	1948-5182 (online)
Open Access	This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (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/
Copyright	© The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
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Category	Gastroenterology & Hepatology
Manuscript Type	Clinical Trials Study
Article Title	Neonatal cholestasis and hepatosplenomegaly caused by congenital dyserythropoietic anemia type 1: A case report
Manuscript Source	Invited Manuscript
All Author List	Catalina Jaramillo, Anna K Ermarth, Angelica R Putnam and Mark Deneau
ORCID	Author(s) ORCID Number Catalina Jaramillo http://orcid.org/0000-0003-0708-8247 Anna K Ermarth http://orcid.org/0000-0003-3688-5624 Angelica R Putnam http://orcid.org/0000-0003-3983-5024 Mark Deneau http://orcid.org/0000-0003-0459-9404
Funding Agency and Grant Number
Corresponding Author	Mark Deneau, MD, MSc, Associate Professor, Department of Pediatrics, University of Utah, 81 North Mario Capecchi Drive, Salt Lake City, UT 84113, United States. mark.deneau@hsc.utah.edu
Key Words	Congenital dyserythropoietic anemia; Hemochromatosis; Pulmonary hypertension; Jaundice; Case report
Core Tip	Congenital dyserythropoietic anemia type 1 (CDA1) is an autosomal recessive disorder of ineffective erythropoiesis, resulting in increased iron storage. We report a rare case of CDA1 with novel genetic mutations, in a newborn presenting with severe anemia, cholestasis and liver failure. This case highlights how liver histology helped confirm the diagnosis.
Publish Date	2019-05-27 08:24
Citation	Jaramillo C, Ermarth AK, Putnam AR, Deneau M. Neonatal cholestasis and hepatosplenomegaly caused by congenital dyserythropoietic anemia type 1: A case report. World J Hepatol 2019; 11(5): 477-482
URL	https://www.wjgnet.com/1948-5182/full/v11/i5/477.htm
DOI	https://dx.doi.org/10.4254/wjh.v11.i5.477

Full Article (PDF)	WJH-11-477.pdf
Full Article (Word)	WJH-11-477.docx
Manuscript File	FP6832_de26_CE1MS-edit2.docx
Answering Reviewers	46996-Answering reviewers.pdf
Audio Core Tip	46996-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	46996-Conflict-of-interest statement.pdf
Copyright License Agreement	46996-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	46996-Informed consent statement.pdf
Supplementary Material	46996-Supplementary material.pdf
Peer-review Report	46996-Peer-review(s).pdf
Scientific Editor Work List	46996-Scientific editor work list.pdf
CrossCheck Report	46996-CrossCheck Report.pdf