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5/27/2019 8:24:36 AM | Browse: 747 | Download: 952
Publication Name World Journal of Hepatology
Manuscript ID 46996
Country/Territory 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 Company 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.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
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