Skip to main content

Main menu

  • Home
  • Content
    • Latest
    • Archive
    • home
  • Info for
    • Authors
    • Reviewers
    • Subscribers
    • Institutions
    • Advertisers
    • Join SMJ
  • About Us
    • About Us
    • Editorial Office
    • Editorial Board
  • More
    • Advertising
    • Alerts
    • Feedback
    • Folders
    • Help
  • Other Publications
    • NeuroSciences Journal

User menu

  • My alerts
  • Log in

Search

  • Advanced search
Saudi Medical Journal
  • Other Publications
    • NeuroSciences Journal
  • My alerts
  • Log in
Saudi Medical Journal

Advanced Search

  • Home
  • Content
    • Latest
    • Archive
    • home
  • Info for
    • Authors
    • Reviewers
    • Subscribers
    • Institutions
    • Advertisers
    • Join SMJ
  • About Us
    • About Us
    • Editorial Office
    • Editorial Board
  • More
    • Advertising
    • Alerts
    • Feedback
    • Folders
    • Help
  • Follow psmmc on Twitter
  • Visit psmmc on Facebook
  • RSS
Brief ReportBrief Communication
Open Access

Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis

An important cause of hypoglycemia in children

Rihab M. Salih, Esraa A. Mohammed, Amal M. Alhashem, Sarar Mohamed and Aida I. Al-aqeel
Saudi Medical Journal February 2020, 41 (2) 199-202; DOI: https://doi.org/10.15537/smj.2020.2.24885
Rihab M. Salih
From the Department of Pediatrics, Medical Genetics and Metabolic Division (Salih, Mohammed, Alhashem, Mohamed, Al-aqeel), Prince Sultan Military Medical City, from the Department of Anatomy and Cell Biology (Alhashem); from the Department of Pediatrics (Mohamed); from the Department of Anatomy and Embryology (Al-aqeel), College of Medicine, Alfaisal University, from the Department of Pediatrics (Mohammed), Prince Abdullah bin Khalid Celiac Disease Research Chair, King Saud University, Riyadh, Kingdom of Saudi Arabia, and from the Department of Biochemistry and Molecular Biology (Al-aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon
MD, ABP
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Esraa A. Mohammed
From the Department of Pediatrics, Medical Genetics and Metabolic Division (Salih, Mohammed, Alhashem, Mohamed, Al-aqeel), Prince Sultan Military Medical City, from the Department of Anatomy and Cell Biology (Alhashem); from the Department of Pediatrics (Mohamed); from the Department of Anatomy and Embryology (Al-aqeel), College of Medicine, Alfaisal University, from the Department of Pediatrics (Mohammed), Prince Abdullah bin Khalid Celiac Disease Research Chair, King Saud University, Riyadh, Kingdom of Saudi Arabia, and from the Department of Biochemistry and Molecular Biology (Al-aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon
MBBS
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Amal M. Alhashem
From the Department of Pediatrics, Medical Genetics and Metabolic Division (Salih, Mohammed, Alhashem, Mohamed, Al-aqeel), Prince Sultan Military Medical City, from the Department of Anatomy and Cell Biology (Alhashem); from the Department of Pediatrics (Mohamed); from the Department of Anatomy and Embryology (Al-aqeel), College of Medicine, Alfaisal University, from the Department of Pediatrics (Mohammed), Prince Abdullah bin Khalid Celiac Disease Research Chair, King Saud University, Riyadh, Kingdom of Saudi Arabia, and from the Department of Biochemistry and Molecular Biology (Al-aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon
MD, FMG
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Sarar Mohamed
From the Department of Pediatrics, Medical Genetics and Metabolic Division (Salih, Mohammed, Alhashem, Mohamed, Al-aqeel), Prince Sultan Military Medical City, from the Department of Anatomy and Cell Biology (Alhashem); from the Department of Pediatrics (Mohamed); from the Department of Anatomy and Embryology (Al-aqeel), College of Medicine, Alfaisal University, from the Department of Pediatrics (Mohammed), Prince Abdullah bin Khalid Celiac Disease Research Chair, King Saud University, Riyadh, Kingdom of Saudi Arabia, and from the Department of Biochemistry and Molecular Biology (Al-aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon
FRCPCH, MD
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Aida I. Al-aqeel
From the Department of Pediatrics, Medical Genetics and Metabolic Division (Salih, Mohammed, Alhashem, Mohamed, Al-aqeel), Prince Sultan Military Medical City, from the Department of Anatomy and Cell Biology (Alhashem); from the Department of Pediatrics (Mohamed); from the Department of Anatomy and Embryology (Al-aqeel), College of Medicine, Alfaisal University, from the Department of Pediatrics (Mohammed), Prince Abdullah bin Khalid Celiac Disease Research Chair, King Saud University, Riyadh, Kingdom of Saudi Arabia, and from the Department of Biochemistry and Molecular Biology (Al-aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon
FRCP, FACMG
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: [email protected]
  • Article
  • Figures & Data
  • eLetters
  • Info & Metrics
  • References
  • PDF
Loading

Article Information

vol. 41 no. 2 199-202
DOI 
https://doi.org/10.15537/smj.2020.2.24885
PubMed 
32020156

Published By 
Saudi Medical Journal
Online ISSN 
1658-3175
History 
  • Received September 3, 2019
  • Accepted December 26, 2019
  • Published online February 1, 2020.

Copyright & Usage 
Copyright: © Saudi Medical Journal This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Author Information

  1. Rihab M. Salih, MD, ABP,
  2. Esraa A. Mohammed, MBBS,
  3. Amal M. Alhashem, MD, FMG,
  4. Sarar Mohamed, FRCPCH, MD and
  5. Aida I. Al-aqeel, FRCP, FACMG⇑
  1. From the Department of Pediatrics, Medical Genetics and Metabolic Division (Salih, Mohammed, Alhashem, Mohamed, Al-aqeel), Prince Sultan Military Medical City, from the Department of Anatomy and Cell Biology (Alhashem); from the Department of Pediatrics (Mohamed); from the Department of Anatomy and Embryology (Al-aqeel), College of Medicine, Alfaisal University, from the Department of Pediatrics (Mohammed), Prince Abdullah bin Khalid Celiac Disease Research Chair, King Saud University, Riyadh, Kingdom of Saudi Arabia, and from the Department of Biochemistry and Molecular Biology (Al-aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon
  1. Address correspondence and reprints request to: Dr. Aida I. Al-aqeel, Department of Pediatrics, Medical Genetics and Metabolic division, Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia. E-mail: aalaqeel{at}psmmc.med.sa ORCHID ID: https://orcid.org/0000-0002-0902-0812
View Full Text

Cited By...

  • 5 Citations
  • 5 Citations
  • Google Scholar

This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • Fructose-1,6-bisphosphatase is a nonenzymatic safety valve that curtails AKT activation to prevent insulin hyperresponsiveness
    Li Gu, Yahui Zhu, Kosuke Watari, Maiya Lee, Junlai Liu, Sofia Perez, Melinda Thai, Joshua E. Mayfield, Bichen Zhang, Karina Cunha e Rocha, Fuming Li, Laura C. Kim, Alexander C. Jones, Igor H. Wierzbicki, Xiao Liu, Alexandra C. Newton, Tatiana Kisseleva, Jun Hee Lee, Wei Ying, David J. Gonzalez, Alan R. Saltiel, M. Celeste Simon, Michael Karin
    Cell Metabolism 2023 35 6
  • Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A)
    Nina Brauer, Yuto Maruta, Miriam Lisci, Katharina Strege, Ilske Oschlies, Hikari Nakamura, Svea Böhm, Kai Lehmberg, Leon Brandhoff, Stephan Ehl, Nima Parvaneh, Wolfram Klapper, Mitsunori Fukuda, Gillian M. Griffiths, Hans Christian Hennies, Tim Niehues, Sandra Ammann
    Frontiers in Immunology 2023 14
  • Fructose-1,6-bisphosphatase deficiency: estimation of prevalence in the Chinese population and analysis of genotype-phenotype association
    Qi Ni, Meiling Tang, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Wenhao Zhou, Xinran Dong
    Frontiers in Genetics 2024 15
  • An extremely rare case of hypoglycemia with a novel mutation and review of the literature: fructose-1,6 bisphosphatase deficiency in an adult man
    Hakan Doğruel, Mustafa Aydemir, Nusret Yılmaz, Ramazan Sarı
    Irish Journal of Medical Science (1971 -) 2024 193 3
  • Intrafamilial phenotypic variability due to a missense pathogenic variant in FBP1 gene
    Setila Dalili, Nasrin Sedighi Pirsaraei, Ameneh Sharifi, Alireza Pouryousef, Fatemeh Aghaee, Reza Bayat, Babak Ghavami, Bahareh Rabbani, Nejat Mahdieh
    Molecular Genetics and Metabolism Reports 2024 41
PreviousNext
Back to top

In this issue

Saudi Medical Journal: 41 (2)
Saudi Medical Journal
Vol. 41, Issue 2
1 Feb 2020
  • Table of Contents
  • Cover (PDF)
  • Index by author
Print
Download PDF
Email Article

Thank you for your interest in spreading the word on Saudi Medical Journal.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis
(Your Name) has sent you a message from Saudi Medical Journal
(Your Name) thought you would like to see the Saudi Medical Journal web site.
Citation Tools
Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis
Rihab M. Salih, Esraa A. Mohammed, Amal M. Alhashem, Sarar Mohamed, Aida I. Al-aqeel
Saudi Medical Journal Feb 2020, 41 (2) 199-202; DOI: 10.15537/smj.2020.2.24885

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis
Rihab M. Salih, Esraa A. Mohammed, Amal M. Alhashem, Sarar Mohamed, Aida I. Al-aqeel
Saudi Medical Journal Feb 2020, 41 (2) 199-202; DOI: 10.15537/smj.2020.2.24885
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Bookmark this article

Jump to section

  • Article
    • Abstract
    • Methods
    • Results
    • Discussion
    • Acknowledgment
    • Footnotes
    • References
  • Figures & Data
  • eLetters
  • References
  • Info & Metrics
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • FBP1 is a nonenzymatic safety valve that curtails AKT activation to prevent insulin hyperresponsiveness
  • Google Scholar

More in this TOC Section

  • Successful management of human parainfluenza virus-3 outbreak in a tertiary neonatal intensive care unit
  • Experience of pediatric liver disease at a university hospital in Western Saudi Arabia
  • Risk of malignancy in thyroid nodules Bethesda III sub classification into nuclear atypia and architectural atypia. A retrospective study
Show more Brief Communication

Similar Articles

Keywords

  • Fructose-1,6-bisphosphatase
  • FBPase
  • FBP1 gene
  • fructose
  • hypoglycemia

CONTENT

  • home

JOURNAL

  • home

AUTHORS

  • home
Saudi Medical Journal

© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

Powered by HighWire