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Updated: Feb 19, 2026

Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
Published on: October 10, 2025
A celiac case mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
Erhan Aksoy1, Serap Tıraş-Teber2, Gülhis Deda2
1Department of Pediatric Neurology, Dr. Sami Ulus Maternity and Childrens' Health and Diseases Training and Research Hospital, Ankara, Turkey.
Abstract:
Celiac disease (CD) is a chronic disease involving a number of systems in addition to gastrointestinal tract. Although not clear, it has been supposed that the neurological symptoms of CD develop due to immune-mediated mechanisms. In this paper, we present a rare case diagnosed with CD at 12 years of age, and presented with a clinical picture resembling mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). She had onset of her neurological symptoms at the age of 6 years, they progressed despite various therapies, and she became wheelchair-bound.

