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Articles Published Processes
8/27/2024 3:11:19 PM | Browse: 47 | Download: 212
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Received |
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2023-12-18 10:06 |
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Peer-Review Started |
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2023-12-18 10:06 |
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To Make the First Decision |
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Return for Revision |
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2024-03-06 03:48 |
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Revised |
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2024-05-29 03:57 |
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Second Decision |
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2024-06-28 02:45 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2024-06-28 08:25 |
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Articles in Press |
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2024-06-28 08:25 |
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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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2024-07-22 02:45 |
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Publish the Manuscript Online |
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2024-08-27 15:11 |
ISSN |
1948-9358 (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 |
Endocrinology & Metabolism |
Manuscript Type |
Editorial |
Article Title |
Exploring the genetic basis of childhood monogenic diabetes
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Manuscript Source |
Invited Manuscript |
All Author List |
Debmalya Sanyal |
ORCID |
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Funding Agency and Grant Number |
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Corresponding Author |
Debmalya Sanyal, FACE, FRCP, MBBS, MD, MRCP, Professor, Department of Endocrinology, KPC Medical College, 1F Raja Subodh Chandra Mullick Road, Kolkata Pin 700032, West Bengal, India. drdebmalyasanyal@gmail.com |
Key Words |
Monogenic diabetes; Genetic mutation; Insulin resistance; Beta-cell function; Diabetes mellitus |
Core Tip |
Monogenic diabetes, a rare yet impactful condition in childhood, results from genetic variations, causing early-onset diabetes. Affecting 1%-5% of children, early detection and tailored genetic treatments can enhance long-term health. Culprits include genetic variations in beta-cell regulatory genes and severe insulin resistance. Identifying specific types allows transitioning to sulfonylureas while maintaining glucose control. Tools to differentiate diabetes types underscore genetic screening's importance for prognosis and treatment guidance. This review delves into genetic insights into childhood monogenic diabetes, offering diagnosis and management guidance for affected youth's better health. |
Publish Date |
2024-08-27 15:11 |
Citation |
<p>Sanyal D. Exploring the genetic basis of childhood monogenic diabetes. <i>World J Diabetes</i> 2024; 15(9): 1829-1832</p> |
URL |
https://www.wjgnet.com/1948-9358/full/v15/i9/1829.htm |
DOI |
https://dx.doi.org/10.4239/wjd.v15.i9.1829 |
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