Fructose malabsorption: causes, diagnosis and treatment
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DOI: 10.1017/s0007114521001215
Abstract: Abstract This review intends to act as an overview of fructose malabsorption (FM) and its role in the aetiology of diseases including, but not limited to, irritable bowel syndrome (IBS) and infantile colic and the… read more here.
Keywords: diagnosis; diagnosis treatment; fructose malabsorption; causes diagnosis ... See more keywords
Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption
Sign Up to like & getrecommendations! Published in 2022 at "BMC Gastroenterology"
DOI: 10.1186/s12876-022-02244-7
Abstract: Background While role of ALDOB- related gene variants for hereditary fructose intolerance is well established, contribution of gene variants for acquired fructose malabsorption (e.g. SLC2A5 , GLUT5) is not well understood. Methods Patients referred to… read more here.
Keywords: fructose malabsorption; gene variants; slc2a5 gene; gene ... See more keywords