Results 141 to 150 of about 1,942 (174)

Monogenic inflammatory bowel disease: An unfolding enigma. [PDF]

World J Clin Pediatr
Ghosh U, Samanta A.
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A Case Report: Cryptogenic Multifocal Ulcerative Stenosing Enteritis - A Diagnostic Challenge Mimicking Crohn's Disease. [PDF]

Case Rep Gastroenterol
Luke N, De Leon IC, Azizi S, Katz S.
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Two cases of primary hypertrophic osteoarthropathy caused by HPGD variants: a case report and literature review. [PDF]

BMC Pediatr
Li J, Jia S, Guo J, Xie W, Ma Y, Gao X, Gao M.   +6 more
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Targeting Metabolomics in Primary Hypertrophic Osteoarthropathy: Uncovering Novel Insights into Disease Pathogenesis.

J Clin Endocrinol Metab
Pang Q, Qi X, Chi Y, Jiajue R, Zhang L, Cui L, Wang O, Li M, Xing X, Jiang Y, Gong Y, Xia W.   +11 more
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Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene

Digestive Diseases and Sciences, 2020
Chronic enteropathy associated with the SLCO2A1 gene (CEAS) is an enteropathy characterized by multiple small intestinal ulcers of nonspecific histology, also known as chronic nonspecific multiple ulcers of the small intestine. The SLCO2A1 gene encodes a prostaglandin transporter (PGT).The aim of this study was to investigate the clinical ...
Hui Huang, Xuehong Wang, Dalian Ou, Xiaowei Liu, Boda Wu, Bai Zhou, Yongjun Wang, Xiaoliu Shi   +7 more
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Chronic enteropathy associated with SLCO2A1 gene: A case report and literature review

Clinics and Research in Hepatology and Gastroenterology, 2019
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 were revealed by endoscopic examination. Computed tomography enterography (CTE) and magnetic resonance enterography (MRE)
Peng, Hu, Huiqin, He, Ning, Dai, Shizheng, Zhang, Liping, Deng   +4 more
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Pachydermoperiostosis of the complete type: A novel missense mutation c.101T > C in the SLCO2A1 gene

European Journal of Medical Genetics, 2017
We report on a rare case of pachydermoperiostosis (PDP) in a 25-year-old male who was admitted to our hospital because of enlargement of fingers and toes. Through examination, we found some typical features on the patient including finger clubbing, periostosis, pachydermia, and cutis verticis gyrata (CVG). But laboratory tests were almost within normal
Wenbin, Ma, Shuqin, Guo, Yan, Li, Zhihong, Li   +3 more
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P868 Clinical features of chronic enteropathy associated with SLCO2A1 gene

Journal of Crohn's and Colitis, 2023
Abstract Background Chronic enteropathy associated with the SLCO2A1 gene (CEAS) is a hereditary disease caused by mutations of the SLCO2A1 gene which encodes a prostaglandin transporter. This disease is rare and intractable characterized by persistent blood and protein loss. There are few reports from
J Umeno, Y Fuyuno, T Torisu, Y Matsuno, M Esaki, S Yanai, N Ohmiya, T Hisamatsu, K Watanabe, N Hosoe, H Ogata, F Hirai, T Hisabe, T Matsui, T Kitazono, T Matsumoto   +15 more
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Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1

Modern Rheumatology Case Reports, 2021
Male, 41 years old (yo) had been complaining of severe arthralgia. Past History indicated obstruction of intestinal tract at 12 yo and gastric ulcer at 13 yo. He had been suffered from polyarthralgia especially at PIP and MP joints of both hands from 38 yo.
Tatsuo, Ishizuka, Kei, Fujioka, Ichiro, Mori, Tomofumi, Takeda, Masayuki, Fuwa, Takahide, Ikeda, Koichiro, Taguchi, Hiroyuki, Morita, Kazuhiko, Nakabayashi, Hironori, Niizeki   +9 more
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The complete type of pachydermoperiostosis: A novel nonsense mutation p.E141* of the SLCO2A1 gene

Journal of Dermatological Science, 2014
H. Niizeki, A. Shiohama, T. Sasaki, A. Seki, K. Kabashima, A. Otsuka, K. Kosaki, A. Ogo, T. Yamada, M. Miyasaka, K. Matsuoka, A. Hirakiyama, T. Okuyama, M. Matsuda, K. Nakabayashi, K. Tanese, A. Ishiko, M. Amagai, J. Kudoh   +18 more
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