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   Articles with "associated slco2a1" as a keyword



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Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn’s disease

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recommendations! Published in 2017 at "Journal of Gastroenterology"

DOI: 10.1007/s00535-017-1426-y

Abstract: BackgroundChronic enteropathy associated with SLCO2A1 gene (CEAS) is a hereditary disease caused by mutations in the SLCO2A1 gene and characterized by multiple small intestinal ulcers of nonspecific histology. SLCO2A1 is also a causal gene of… read more here.

Keywords: clinical features; slco2a1 gene; disease; enteropathy associated ... See more keywords
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Chronic enteropathy associated with SLCO2A1 gene: A case report and literature review.

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recommendations! Published in 2019 at "Clinics and research in hepatology and gastroenterology"

DOI: 10.1016/j.clinre.2019.05.003

Abstract: A case of chronic enteropathy associated with SLCO2A1 gene (CEAS) is presented. The female patient was readmitted four times during a three-year follow-up period for intractable dropsy and anemia. Multiple ulcers of small bowel wall… read more here.

Keywords: slco2a1 gene; case; enteropathy associated; gene ... See more keywords
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A Novel Chronic Enteropathy Associated with SLCO2A1 Gene Mutation: Enterography Findings in a Multicenter Korean Registry

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recommendations! Published in 2023 at "Korean Journal of Radiology"

DOI: 10.3348/kjr.2022.0684

Abstract: Objective Chronic enteropathy associated with SLCO2A1 gene (CEAS) is a recently recognized disease. We aimed to evaluate the enterographic findings of CEAS. Materials and Methods Altogether, 14 patients with CEAS were confirmed based on known… read more here.

Keywords: associated slco2a1; chronic enteropathy; enterography; multicenter korean ... See more keywords
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Distinction between Chronic Enteropathy Associated with the SLCO2A1 Gene and Crohn’s Disease

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recommendations! Published in 2019 at "Gut and Liver"

DOI: 10.5009/gnl18261

Abstract: Background/Aims We recently identified recessive mutations in the solute carrier organic anion transporter family member 2A1 gene (SLCO2A1) as causative variants of chronic nonspecific multiple ulcers of the small intestine (chronic enteropathy associated with SLCO2A1,… read more here.

Keywords: associated slco2a1; enteropathy associated; patients ceas; gene ... See more keywords