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12/19/2024 6:09:11 AM | Browse: 121 | Download: 196
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Received |
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2024-08-10 09:23 |
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Peer-Review Started |
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2024-08-10 09:23 |
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To Make the First Decision |
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Return for Revision |
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2024-10-25 02:58 |
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Revised |
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2024-11-06 13:31 |
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Second Decision |
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2024-12-02 02:44 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2024-12-02 07:54 |
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Articles in Press |
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2024-12-02 07:54 |
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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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2024-12-11 05:02 |
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Publish the Manuscript Online |
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2024-12-19 01:57 |
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) 2025. 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 |
Hematology |
Manuscript Type |
Minireviews |
Article Title |
Beta thalassemia syndromes: New insights
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Manuscript Source |
Invited Manuscript |
All Author List |
Ana Dordevic, Ines Mrakovcic-Sutic, Sonja Pavlovic, Milena Ugrin and Jelena Roganovic |
Funding Agency and Grant Number |
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Corresponding Author |
Jelena Roganovic, MD, PhD, Department of Pediatric Hematology and Oncology, Children’s Hospital Zagreb, Klaiceva 16, Zagreb 10000, Croatia. jelena.roganovic@kdb.hr |
Key Words |
Beta thalassemia; Hemoglobin; Molecular defects; Ineffective erythropoiesis; Hemolysis; Transfusion; Iron chelation; Novel therapies |
Core Tip |
Beta thalassemia syndromes are among the most common monogenic disorders worldwide, characterized by impaired hemoglobin synthesis that leads to ineffective erythropoiesis, chronic hemolysis, iron overload, and subsequent complications. The clinical manifestations are diverse, as a result of the underlying beta-globin gene variants and the coinheritance of modifying factors. Recent advances in the understanding of the underlying molecular and cellular mechanisms have facilitated the development of novel therapeutic strategies. The purpose of this article is to briefly describe new insights in the pathophysiology of this old disease, and discuss revolutionary changes in the treatment landscape for severe forms of beta thalassemia. |
Publish Date |
2024-12-19 01:57 |
Citation |
<p>Dordevic A, Mrakovcic-Sutic I, Pavlovic S, Ugrin M, Roganovic J. Beta thalassemia syndromes: New insights. <i>World J Clin Cases</i> 2025; 13(10): 100223</p> |
URL |
https://www.wjgnet.com/2307-8960/full/v13/i10/100223.htm |
DOI |
https://dx.doi.org/10.12998/wjcc.v13.i10.100223 |
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