Results 111 to 120 of about 509 (131)

[Three cases of chronic enteropathy associated with SLCO2A1 gene in children].

Zhonghua er ke za zhi = Chinese journal of pediatrics, 2023
W. Lin, F. F. Wang, J. Xie, L. Ren, Y. Han, L. N. Sun, P. Y. Chen, S. Gong, Y. Fang, L. Geng   +9 more
semanticscholar   +3 more sources

[Chronic enteropathy associated with SLCO2A1 gene (CEAS)].

Nihon Shokakibyo Gakkai zasshi = The Japanese journal of gastro-enterology, 2022
J. Umeno, K. Uchida, Takayuki Matsumoto
semanticscholar   +3 more sources

Chronic enteropathy associated with SLCO2A1 gene (CEAS) in Indian adolescents: Apropos of two cases

Indian Journal of Gastroenterology
Aditi Kumar, Janvi Sirwani, T. P. Tripathy, S. Patra, M. Panigrahi, D. Sahoo, Sonali Mohapatra, A. Satapathy   +7 more
semanticscholar   +3 more sources

S4976 Misdiagnosed as Crohn's: A Case Report of Chronic Enteropathy Associated With the SLCO2A1 Gene

American Journal of Gastroenterology
Hayalneh Gessessew, N. Sharif, Thanita Thongtan, Heba N. Iskandar   +3 more
semanticscholar   +2 more sources

P-174 Chronic Enteropathy Associated with SLCO2A1 Gene, Encoding Prostaglandin Transporter (CEAS)

Inflammatory Bowel Diseases, 2016
Junji Umeno, Tadakazu Hisamatsu, Motohiro Esaki, Atsushi Hirano, Shuji Kochi, Kenji Watanabe, Kunihiko Aoyagi, Fumihito Hirai, Toshiyuki Matsui, Tsuneyoshi Yao, Toshifumi Hibi, Takanori Kanai, Takayuki Matsumoto, Takanari Kitazono   +13 more
openaire   +2 more sources

Chronic Enteropathy Associated with SLCO2A1 Gene (CEAS)

exaly   +2 more sources

Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review

American Journal of Medical Genetics. Part A, 2023
Autosomal recessive type 2 primary hypertrophic osteoarthropathy (PHOAR2) and chronic enteropathy associated with SLCO2A1 (CEAS) are two entities caused by pathogenic variants (PVs) in the SLCO2A1 gene that can coexist or occur independently from one ...
Tamara N. Kimball, Pamela Rivero-García, A. Barrera-Godínez, J. Domínguez-Cherit   +3 more
semanticscholar   +1 more source

Attenuated Expression of SLCO2A1 Caused by DNA Methylation in Pediatric Inflammatory Bowel Disease.

Inflammatory Bowel Diseases, 2023
BACKGROUND SLCO2A1 encodes a prostaglandin (PG) transporter, and autosomal recessive pathogenic variants of this gene cause chronic enteropathy associated with SLCO2A1.
Natsuki Ito, T. Kudo, H. Eguchi, Keisuke Jimbo, A. Furuhata, T. Okuno, I. Takeuchi, K. Arai, T. Ishige, Yasushi Okazaki, Toshiaki Shimizu   +10 more
semanticscholar   +1 more source

Cryptogenic multifocal ulcerating stenosing enteritis and other under-recognised small bowel inflammatory enteropathies

Current Opinion in Gastroenterology, 2022
Purpose of review Capsule endoscopy and more sensitive radiological techniques have resulted in more enteropathies being detected. A rare disease of unknown aetiology, ‘cryptogenic multifocal ulcerating stenosing enteritis’ or ‘chronic nonspecific ...
M. McAlindon
semanticscholar   +1 more source

Acetaminophen as a possible treatment option for pachydermoperiostosis carrying mutated SLCO2A1: Case series

Journal of dermatology (Print)
Pachydermoperiostosis (PDP) is a genetic disease characterized by digital clubbing, periostosis, and pachydermia. PDP with these three features, along with cutis verticis gyrata (CVG), is categorized as the “complete form,” whereas cases without CVG are ...
T. Takegami, Mami I Mamiya, S. Yonekura, K. Yoshida, Ryo Tanaka, Kazuhiko Nakabayashi, H. Niizeki, Takashi Nomura, K. Kabashima   +8 more
semanticscholar   +1 more source