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Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
Published on: October 10, 2025
Mitochondrial encephalomyopathy caused by a novel ACAD9 mutation: a case report
Shuo Li1, Yijun Li1, Yonghua Chen2
1The First Clinical Medical College of Anhui University of Chinese Medicine, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui, China.
This study identifies novel ACAD9 gene variants in a patient with mitochondrial encephalomyopathy, highlighting the importance of genetic sequencing for diagnosing complex neurological disorders.
Area of Science:
- Genetics
- Neurology
- Mitochondrial Diseases
Background:
- A 27-year-old male presented with global developmental delay, hearing loss, ataxia, dysarthria, and intellectual disability following perinatal hypoxia.
- Clinical presentation suggested a progressive multisystem disorder.
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