Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient

Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient

<div><p>Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized mainly by the accumulation of glycogen in the liver and kidney. It is inherited as an autosomal recessive disorder caused by mutations in the SLC2A2 gene, which encodes for GLUT2. Pa...

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Bibliographic Details
Main Author: Sanaa Sharari (12561952) (author)
Other Authors: Mustapha Aouida (417652) (author), Idris Mohammed (751020) (author), Basma Haris (12040355) (author), Ajaz Ahmad Bhat (12561955) (author), Iman Hawari (12561958) (author), Sabah Nisar (12561961) (author), Igor Pavlovski (12561964) (author), Kabir H. Biswas (5705864) (author), Najeeb Syed (12561967) (author), Selma Maacha (501715) (author), Jean-Charles Grivel (284645) (author), Maryam Saifaldeen (12561970) (author), Johan Ericsson (49714) (author), Khalid Hussain (110443) (author)
Published: 2022
Subjects:
Biomedical and clinical sciences
Clinical sciences
Fanconi-Bickel syndrome (FBS)
dysglycemia
glucose transporter 2 (GLUT2)
clustered regularly interspaced short palindromic repeats (CRISPR)- Cas9
sodium-glucose transport protein 2 (SGLT2)
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