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9/27/2024 11:48:17 AM | Browse: 155 | Download: 285
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Received |
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2024-03-06 08:21 |
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Peer-Review Started |
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2024-03-06 08:21 |
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To Make the First Decision |
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Return for Revision |
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2024-07-23 04:47 |
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Revised |
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2024-08-03 12:09 |
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Second Decision |
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2024-09-18 02:41 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2024-09-19 10:35 |
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Articles in Press |
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2024-09-19 10:35 |
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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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2024-09-23 02:29 |
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Publish the Manuscript Online |
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2024-09-27 08:43 |
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: https://creativecommons.org/licenses/by-nc/4.0/ |
Copyright |
© The Author(s) 2024. 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 |
Genetics & Heredity |
Manuscript Type |
Letter to the Editor |
Article Title |
Tricuspid mass-curious case of Li-Fraumeni syndrome: A letter to the editor
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Manuscript Source |
Invited Manuscript |
All Author List |
Mohammad S Al-Haggar and Zahraa A Abdelmoneim |
Funding Agency and Grant Number |
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Corresponding Author |
Zahraa A Abdelmoneim, MD, Lecturer, Department of Pediatrics, Genetic Unit, Mansoura University Children Hospital, EL Gomhoria Street, Mansoura 35516, Egypt. hzahraa211@gmail.com |
Key Words |
Li-Fraumeni syndrome; Cancers; Cardiac thrombus; Genetic counseling; Surveillance |
Core Tip |
Li-Fraumeni syndrome (LFS) is an inherited propensity to various distinct, frequently uncommon malignancies. Pediatric and adolescent age groups are more likely to acquire many malignancies, including soft-tissue and bone tumors, breast cancer, central nervous system cancers, adrenocortical carcinoma, and blood cancers. LFS individuals may also develop various types of cancer, including gastrointestinal, lung, kidney, thyroid, and skin cancers, as well as those affecting the gonadal organs. An accurate diagnosis of LFS is critical for afflicted families to receive appropriate genetic counseling and be monitored for early cancer detection. |
Publish Date |
2024-09-27 08:43 |
Citation |
<p>Al-Haggar MS, Abdelmoneim ZA. Tricuspid mass-curious case of Li-Fraumeni syndrome: A letter to the editor. <i>World J Clin Cases</i> 2024; 12(33): 6644-6646</p> |
URL |
https://www.wjgnet.com/2307-8960/full/v12/i33/6644.htm |
DOI |
https://dx.doi.org/10.12998/wjcc.v12.i33.6644 |
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