Functional variants in the sucrase–isomaltase gene associate with increased risk of irritable bowel syndrome
Maria Henström, Lena Diekmann, Ferdinando Bonfiglio, Fatemeh Hadizadeh et autres
Objective IBS is a common gut disorder of uncertain pathogenesis. Among other factors, genetics and certain foods are proposed to contribute. Congenital sucrase–isomaltase deficiency (CSID) is a rare genetic form of disaccharide malabsorption characterised by diarrhoea, abdominal pain and bloating, which are …
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