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7/7/2022 10:42:01 AM | Browse: 224 | Download: 577
Publication Name World Journal of Clinical Pediatrics
Manuscript ID 73611
Country India
Received
2021-11-27 16:49
Peer-Review Started
2021-11-27 16:53
To Make the First Decision
Return for Revision
2022-04-15 12:09
Revised
2022-05-08 05:44
Second Decision
2022-06-15 02:59
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2022-06-20 20:54
Articles in Press
2022-06-20 20:54
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2022-06-22 09:38
Publish the Manuscript Online
2022-07-06 13:21
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 ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Gastroenterology & Hepatology
Manuscript Type Minireviews
Article Title Hereditary fructose intolerance: A comprehensive review
Manuscript Source Invited Manuscript
All Author List Sumit Kumar Singh and Moinak Sen Sarma
Funding Agency and Grant Number
Corresponding Author Moinak Sen Sarma, MD, Associate Professor, Pediatric Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raebareli Road, Lucknow 226014, India. moinaksen@yahoo.com
Key Words Hereditary; Fructose; Intolerance; Children; Liver; Steatohepatitis; Aldolase
Core Tip Hereditary Fructose Intolerance is a rare autosomal recessive inherited disorder due to the mutation of enzyme aldolase B. Awareness regarding its diverse manifestations is required to clinically suspect and diagnose this condition. Genetic testing clinches the diagnosis. Treatment is simple and involves only the dietary exclusion of fructose, sucrose and sorbitol. The prognosis is favourable. This review provides a comprehensive understanding of the disease.
Publish Date 2022-07-06 13:21
Citation Singh SK, Sarma MS. Hereditary fructose intolerance: A comprehensive review. World J Clin Pediatr 2022; 11(4): 321-329
URL https://www.wjgnet.com/2219-2808/full/v11/i4/321.htm
DOI https://dx.doi.org/10.5409/wjcp.v11.i4.321
Full Article (PDF) WJCP-11-321.pdf
Full Article (Word) WJCP-11-321.docx
Manuscript File 73611_Auto_Edited_LM.docx
Answering Reviewers 73611-Answering reviewers.pdf
Audio Core Tip 73611-Audio core tip.aac
Conflict-of-Interest Disclosure Form 73611-Conflict-of-interest statement.pdf
Copyright License Agreement 73611-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate 73611-Language certificate.pdf
Peer-review Report 73611-Peer-review(s).pdf
Scientific Misconduct Check 73611-Bing-Liu JH-2.jpg
Scientific Misconduct Check 73611-CrossCheck.jpg
Scientific Editor Work List 73611-Scientific editor work list.pdf