Publication Name	World Journal of Clinical Pediatrics
Manuscript ID	103415
Country	India

Received	2024-11-20 04:45
Peer-Review Started	2024-11-20 04:45
To Make the First Decision
Return for Revision	2025-02-18 07:17
Revised	2025-03-08 03:14
Second Decision	2025-03-17 02:38
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2025-03-17 09:08
Articles in Press	2025-03-17 09:08
Publication Fee Transferred
Edit the Manuscript by Language Editor	2025-03-23 22:58
Typeset the Manuscript	2025-04-30 09:27
Publish the Manuscript Online	2025-06-16 10:38

ISSN	2219-2808 (online)
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Category	Gastroenterology & Hepatology
Manuscript Type	Editorial
Article Title	Hepatic glycogen storage disease: Deciphering the genotype-phenotype conundrum
Manuscript Source	Invited Manuscript
All Author List	Arghya Samanta and Gautam Ray
ORCID	Author(s) ORCID Number Arghya Samanta http://orcid.org/0000-0002-1768-0263 Gautam Ray http://orcid.org/0000-0003-3024-149X
Funding Agency and Grant Number
Corresponding Author	Arghya Samanta, Assistant Professor, Department of Pediatric Gastroenterology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, Uttar Pradesh, India. arghyasamanta29051989@gmail.com
Key Words	Hepatic glycogen storage disease; Genotype-phenotype correlation; Children; Next-generation sequencing; Metabolic control
Core Tip	Glycogen storage diseases (GSDs) are a group of clinically and genetically heterogeneous diseases. The various subtypes of hepatic GSDs are often clinically overlapping, especially in hepatic GSDs. Early diagnosis and proper dietary therapy is paramount for optimal clinical outcome. Certain clinical features and laboratory derangements such as hypoglycemia, elevated liver enzymes and abnormal lipid profile are helpful in diagnosis. Liver biopsy is an invasive diagnostic test, which has been replaced by genetic testing recently. Next-generation sequencing is now being used more frequently for definitive diagnosis of GSD.
Publish Date	2025-06-16 10:38
Citation	<p>Samanta A, Ray G. Hepatic glycogen storage disease: Deciphering the genotype-phenotype conundrum. <i>World J Clin Pediatr</i> 2025; 14(3): 103415</p>
URL	https://www.wjgnet.com/2219-2808/full/v14/i3/103415.htm
DOI	https://dx.doi.org/10.5409/wjcp.v14.i3.103415

Full Article (PDF)	WJCP-14-103415-with-cover.pdf
Manuscript File	103415_Auto_Edited_084846.docx
Answering Reviewers	103415-answering-reviewers.pdf
Audio Core Tip	103415-audio.aac
Conflict-of-Interest Disclosure Form	103415-conflict-of-interest-statement.pdf
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Non-Native Speakers of English Editing Certificate	103415-non-native-speakers.pdf
Peer-review Report	103415-peer-reviews.pdf
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Scientific Editor Work List	103415-scientific-editor-work-list.pdf
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