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

作者信息

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

机构信息

Department of Gastroenterology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.

Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

J Dig Dis. 2024 Sep-Oct;25(9-10):624-631. doi: 10.1111/1751-2980.13317. Epub 2024 Dec 18.

DOI:10.1111/1751-2980.13317
PMID:39694028
Abstract

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%).

摘要

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