罕见消化系统疾病：线粒体神经胃肠道脑肌病，文献综述。

IF 2.3 3区医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of Digestive Diseases Pub Date : 2024-12-18 DOI:10.1111/1751-2980.13317

Ying Hao Sun, Xiao Yin Bai, Tao Guo, Si Yuan Fan, Ge Chong Ruan, Wei Xun Zhou, Hong Yang

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摘要

诊断为线粒体神经胃肠道脑肌病的患者中位年龄为25岁。最常见的神经症状是白质脑病（83.1%）、多神经病变（68.5%）和上睑下垂/眼麻痹（61.8%）。最常见的消化系统症状为体重减轻/恶病质（71.9%）、腹痛（58.4%）、腹泻（57.3%）、呕吐（53.9%）和便秘（13.5%）。

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Rare digestive disease: Mitochondrial neurogastrointestinal encephalomyopathy, review of the literature

The median age of patients at diagnosis of mitochondrial neurogastrointestinal encephalomyopathy was 25 years. The most common neurological symptoms were leukoencephalopathy (83.1%), polyneuropathy (68.5%), and ptosis/ophthalmoparesis (61.8%). And the most common digestive symptoms were weight loss/cachexia (71.9%), abdominal pain (58.4%), diarrhea (57.3%), vomiting (53.9%), and constipation (13.5%).

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来源期刊

Journal of Digestive Diseases 医学-胃肠肝病学

CiteScore

5.40

自引率

2.90%

发文量

审稿时长

6-12 weeks

期刊介绍： The Journal of Digestive Diseases is the official English-language journal of the Chinese Society of Gastroenterology. The journal is published twelve times per year and includes peer-reviewed original papers, review articles and commentaries concerned with research relating to the esophagus, stomach, small intestine, colon, liver, biliary tract and pancreas.