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Articles Published Processes
5/27/2019 8:24:36 AM | Browse: 1065 | Download: 1897
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Received |
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2019-03-11 06:14 |
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Peer-Review Started |
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2019-03-12 09:26 |
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First Decision by Editorial Office Director |
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2019-04-03 23:25 |
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Return for Revision |
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2019-04-10 08:20 |
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Revised |
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2019-04-12 17:49 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2019-04-19 07:45 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2019-04-19 20:35 |
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Articles in Press |
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2019-04-19 20:35 |
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Edit the Manuscript by Language Editor |
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2019-04-25 13:58 |
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Typeset the Manuscript |
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2019-05-25 07:09 |
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Publish the Manuscript Online |
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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
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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| 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
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| Manuscript Source |
Invited Manuscript |
| All Author List |
Catalina Jaramillo, Anna K Ermarth, Angelica R Putnam and Mark Deneau |
| ORCID |
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| Funding Agency and Grant Number |
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| 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 |
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