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

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
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.
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

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

ISSN	1948-5182 (online)
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