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Articles Published Processes
4/30/2020 3:27:12 PM | Browse: 711 | Download: 1018
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Received |
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2020-01-15 10:38 |
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Peer-Review Started |
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2020-01-15 10:38 |
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To Make the First Decision |
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2020-03-05 02:16 |
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Return for Revision |
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2020-03-05 02:19 |
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Revised |
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2020-03-26 12:32 |
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Second Decision |
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2020-04-16 07:34 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Company Editor-in-Chief |
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2020-04-16 23:00 |
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Articles in Press |
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2020-04-16 23:00 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2020-04-28 07:08 |
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Publish the Manuscript Online |
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2020-04-30 15:27 |
| 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/ |
| Copyright |
© The Author(s) 2020. 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 |
Case Report |
| Article Title |
Cholesteryl ester storage disease of clinical and genetic characterisation: A case report and review of literature
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Elias Badal Rashu, Anders Ellekær Junker, Karen Vagner Danielsen, Emilie Dahl, Ole Hamberg, Line Borgwardt, Vibeke Brix Christensen, Nicolai J Wewer Albrechtsen and Lise L Gluud |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Lise L Gluud, DSc, MD, Chief Doctor, Professor, Gastrounit, Copenhagen University Hospital Hvidovre, Kettegaard Alle 30, Hvidovre 2650, Denmark. lise.lotte.gluud.01@regionh.dk |
| Key Words |
Lysosomal acid lipase deficiency; Lysosomal storage disease; Non-alcoholic fatty liver disease; Liver transplantation; Sebelipase alfa; Case report |
| Core Tip |
Cholesteryl ester storage disease is a multisystemic disease affecting several organs. Accordingly, the disease will progress after liver transplantation and may recur in the transplanted liver. Abnormal lipid accumulation in the vascular endothelium causes cardiovascular diseases. The occurrence of single nucleotide polymorphisms associated with fatty liver disease may increase the risk of cirrhosis and of recurrence of fatty liver disease after transplantation. Our case presents findings that underline the importance of monitoring and treatment. |
| Publish Date |
2020-04-30 15:27 |
| Citation |
Rashu EB, Junker AE, Danielsen KV, Dahl E, Hamberg O, Borgwardt L, Christensen VB, Wewer Albrechtsen NJ, Gluud LL. Cholesteryl ester storage disease of clinical and genetic characterisation: A case report and review of literature. World J Clin Cases 2020; 8(9): 1642-1650 |
| URL |
https://www.wjgnet.com/2307-8960/full/v8/i9/1642.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v8.i9.1642 |
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