©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jul 7, 2023; 29(25): 3932-3963
Published online Jul 7, 2023. doi: 10.3748/wjg.v29.i25.3932
Published online Jul 7, 2023. doi: 10.3748/wjg.v29.i25.3932
Glycogen storage diseases: An update
Ersin Gümüş, Hasan Özen, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Hacettepe University Faculty of Medicine, Ihsan Dogramaci Children’s Hospital, Ankara 06230, Turkey
Author contributions: Both authors contributed all parts of the study.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Corresponding author: Hasan Özen, MD, Professor, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Hacettepe University Faculty of Medicine, Ihsan Dogramaci Children’s Hospital, Gevher Nesibe Cad., Ankara 06230, Turkey. haozen@hacettepe.edu.tr
Received: December 28, 2022
Peer-review started: December 28, 2022
First decision: February 1, 2023
Revised: February 15, 2023
Accepted: April 30, 2023
Article in press: April 30, 2023
Published online: July 7, 2023
Processing time: 181 Days and 20.2 Hours
Peer-review started: December 28, 2022
First decision: February 1, 2023
Revised: February 15, 2023
Accepted: April 30, 2023
Article in press: April 30, 2023
Published online: July 7, 2023
Processing time: 181 Days and 20.2 Hours
Core Tip
Core Tip: Glycogen storage diseases are multisystemic diseases that can present at any age. Primarily affected organs are liver and skeletal muscle, but heart, central nervous system, kidneys, intestines, and other organs may also be affected. As the initial presenting symptoms can occur in adulthood, it is a group of rare diseases that should be recognized and managed by not only pediatricians but also physicians taking care of adults.