Chronic Enteropathy Associated with <i>Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1)</i> with Positive Immunohistochemistry for SLCO2A1 Protein-Reference-Cited by-同舟云学术

Chronic Enteropathy Associated with <i>Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1)</i> with Positive Immunohistochemistry for SLCO2A1 Protein

Published:2022-09-01 Issue:17 Volume:61 Page:2607-2611
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Ariake Chizuru¹,Hosoe Naoki¹,Sakurai Hinako²,Tojo Anna²,Hayashi Yukie²,JL Limpias Kamiya Kenji²,Sujino Tomohisa¹,Takabayashi Kaoru¹,Kosaki Kenjiro³,Seki Satowa⁴,Hisamatsu Tadakazu⁴,Ogata Haruhiko¹,Kanai Takanori²

Affiliation:

1. Center for Diagnostic and Therapeutic Endoscopy, Keio University School of Medicine, Japan

2. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Japan

3. Center for Medical Genetics, Keio University School of Medicine, Japan

4. Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/61/17/61_8939-21/_pdf

Reference16 articles.

1. 1. Umeno J, Hisamatsu T, Esaki M, et al. A hereditary enteropathy caused by mutations in the SLCO2A1 gene, encoding a prostaglandin transporter. PLOS Genet 11: e1005581, 2015.

2. 2. Umeno J, Esaki M, Hirano A, et al. Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn's disease. J Gastroenterol 53: 907-915, 2018.

3. 3. Oba MS, Murakami Y, Nishiwaki Y, et al. Estimated prevalence of Cronkhite-Canada syndrome, chronic enteropathy associated with SLCO2A1 gene, and intestinal Behçet's disease in Japan in 2017: a nationwide survey. J Epidemiol 31: 139-144, 2021.

4. 4. Fang Y, Gu W, Luo Y, Chen J. Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report. BMC Pediatr 20: 438, 2020.

5. 5. Hu P, He H, Dai N, Zhang S, Deng L. Chronic enteropathy associated with SLCO2A1 gene: a case report and literature review. Clin Res Hepatol Gastroenterol 43: e68-e72, 2019.

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