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Articles Published Processes
8/3/2026 1:23:48 AM | Browse: 2 | Download: 0
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Received |
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2025-12-10 00:50 |
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Peer-Review Started |
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2025-12-10 00:50 |
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First Decision by Editorial Office Director |
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2026-01-07 02:04 |
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Return for Revision |
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2026-01-07 02:04 |
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Revised |
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2026-01-17 20:34 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2026-03-10 02:37 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2026-03-10 03:35 |
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Articles in Press |
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2026-03-10 03:35 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2026-07-08 06:10 |
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Publish the Manuscript Online |
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2026-08-03 01:23 |
| ISSN |
2219-2808 (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 |
©Author(s) (or their employer(s)) 2026. No commercial re-use. See Permissions. Published by Baishideng Publishing Group Inc. |
| 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 |
Pediatrics |
| Manuscript Type |
Case Report |
| Article Title |
Glycogen storage disease type XIV in the Middle East and North Africa region: A multisystem pediatric case report
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| Manuscript Source |
Invited Manuscript |
| All Author List |
Khalid Adel Al Dojan, Samia Aziz Sulaiman and Abdallah Alaarag |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Samia Aziz Sulaiman, MD, School of Medicine, The University of Jordan, Queen Rania Street, Amman 11942, Jordan. samia.sulaiman2003@gmail.com |
| Key Words |
Glycogen storage disease; Genetic testing; Whole exome sequencing; Phosphoglucomutase-1 deficiency; Case report |
| Core Tip |
Phosphoglucomutase-1 deficiency is a rare, under-recognized disorder with a broad and often subtle multisystem presentation. The condition was first recognized in 1963 through paternity testing and later classified as glycogen storage disease type XIV after reports of glycogen accumulation, severe enzyme deficiency, and rhabdomyolysis. This case underscores the importance of considering phosphoglucomutase-1 deficiency in children with unexplained hepatic dysfunction, hypoglycemia, neuromuscular symptoms, and congenital anomalies, and highlights the diagnostic value of early genomic testing. |
| Publish Date |
2026-08-03 01:23 |
| Citation |
Al Dojan KA, Sulaiman SA, Alaarag A. Glycogen storage disease type XIV in the Middle East and North Africa region: A multisystem pediatric case report. World J Clin Pediatr 2026; 15(9): 117375
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| URL |
https://www.wjgnet.com/2219-2808/full/v15/i3/117375.htm |
| DOI |
https://doi.org/10.5409/wjcp.v15.i3.117375 |
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