一名中国患者出现伴有SLCO2A1和PLA2G4A突变的多发性小肠溃疡。 - Suppr

Multiple small intestinal ulcers with SLCO2A1 and PLA2G4A mutation in a Chinese patient.

作者信息

Sun Kaidi, He Qijin, Zhu Lanping, Abula Gulisitan, Zhao Jingwen, Chen Xin

机构信息

Department of Gastroenterology and Hepatology, Tianjin Medical University General Hospital, No. 154, Anshan Road, Heping District, Tianjin 300052, China.

出版信息

Dig Liver Dis. 2021 Aug;53(8):1062-1064. doi: 10.1016/j.dld.2021.04.032. Epub 2021 May 26.

DOI:10.1016/j.dld.2021.04.032

PMID:34052181

Abstract

摘要

相似文献

Multiple small intestinal ulcers with SLCO2A1 and PLA2G4A mutation in a Chinese patient.一名中国患者出现伴有SLCO2A1和PLA2G4A突变的多发性小肠溃疡。

Dig Liver Dis. 2021 Aug;53(8):1062-1064. doi: 10.1016/j.dld.2021.04.032. Epub 2021 May 26.

Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene.三种中国慢性肠病相关 SLCO2A1 基因患者中发现的 SLCO2A1 基因四种变体。

Dig Dis Sci. 2021 Sep;66(9):2992-3001. doi: 10.1007/s10620-020-06629-0. Epub 2020 Sep 30.

Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene.中国慢性肠病相关 SLCO2A1 基因患者的临床和遗传特征。

Orphanet J Rare Dis. 2024 May 16;19(1):201. doi: 10.1186/s13023-024-03177-y.

Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn's disease.慢性肠病与 SLCO2A1 基因相关的临床特征：一种与克罗恩病在临床上明显不同的新实体。

J Gastroenterol. 2018 Aug;53(8):907-915. doi: 10.1007/s00535-017-1426-y. Epub 2018 Jan 8.

Pathogenesis of chronic enteropathy associated with the gene: Hypotheses and conundrums.与基因相关的慢性肠病的发病机制：假说与困惑。

World J Gastroenterol. 2024 May 21;30(19):2505-2511. doi: 10.3748/wjg.v30.i19.2505.

Chronic Enteropathy Associated With SLCO2A1 Gene [CEAS]-Characterisation of an Enteric Disorder to be Considered in the Differential Diagnosis of Crohn's Disease.慢性肠病相关的 SLCO2A1 基因 [CEAS]-一种需要在克罗恩病鉴别诊断中考虑的肠道疾病的特征。

J Crohns Colitis. 2017 Oct 1;11(10):1277-1281. doi: 10.1093/ecco-jcc/jjx068.

Multiple small intestinal ulcers with SLCO2A1 mutation in a Chinese patient.一名中国患者出现伴有SLCO2A1突变的多处小肠溃疡。

Dig Liver Dis. 2023 Jan;55(1):135-136. doi: 10.1016/j.dld.2022.09.012. Epub 2022 Oct 12.

Cryptogenic Multifocal Ulcerating Stenosing Enteropathy(CMUSE) and/or Chronic Non-specific Multiple Ulcers of the Small Intestine(CNSU) and Non-granulomatous Ulcerating Jejunoileitis (NGUJI).隐源性多灶性溃疡性狭窄性小肠病（CMUSE）和/或慢性非特异性小肠多发性溃疡（CNSU）以及非肉芽肿性溃疡性空回肠炎（NGUJI）。

Curr Gastroenterol Rep. 2019 Sep 10;21(10):53. doi: 10.1007/s11894-019-0721-6.

[Chronic nonspecific multiple ulcers of the small intestine (CNSU) and chronic enteropathy associated with SLCO2A1 (CEAS)].[小肠慢性非特异性多发性溃疡（CNSU）和与SLCO2A1相关的慢性肠病（CEAS）]

Nihon Shokakibyo Gakkai Zasshi. 2016 Aug;113(8):1380-5. doi: 10.11405/nisshoshi.113.1380.

Crohn-like Disease Affecting Small Bowel Due to Monogenic SLCO2A1 Mutations: First Cases of Chronic Enteropathy Associated with SLCO2A1 Gene [CEAS] in France.由于单基因 SLCO2A1 突变导致的小肠克罗恩样疾病：法国首例 SLCO2A1 基因相关慢性肠病 [CEAS]

J Crohns Colitis. 2023 May 3;17(5):816-820. doi: 10.1093/ecco-jcc/jjac181.

引用本文的文献

Chronic Enteropathy Associated with Gene.与基因相关的慢性肠病

Inflamm Intest Dis. 2025 Jun 24;10(1):193-203. doi: 10.1159/000546888. eCollection 2025 Jan-Dec.

Characteristics of chronic enteropathy associated with SLCO2A1 gene (CEAS) in children, a unique type of monogenic very early-onset inflammatory bowel disease.儿童慢性肠病相关 SLCO2A1 基因（CEAS）的特征，一种独特的单基因极早发性炎症性肠病。

BMC Pediatr. 2024 Jun 18;24(1):396. doi: 10.1186/s12887-024-04877-x.

First case report of dichorionic diamniotic twins with chronic enteropathy associated with the SLCO2A1 gene.首例 SLCO2A1 基因相关慢性肠病的双绒毛膜双羊膜双胞胎病例报告。

Clin J Gastroenterol. 2024 Apr;17(2):240-243. doi: 10.1007/s12328-023-01912-9. Epub 2024 Jan 30.

Chronic Enteropathy Associated with Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) with Positive Immunohistochemistry for SLCO2A1 Protein.伴有溶质载体有机阴离子转运家族成员 2A1（SLCO2A1）免疫组织化学阳性的慢性肠病。

Intern Med. 2022 Sep 1;61(17):2607-2611. doi: 10.2169/internalmedicine.8939-21. Epub 2022 Feb 19.

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Multiple small intestinal ulcers with SLCO2A1 and PLA2G4A mutation in a Chinese patient.

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