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Anti-AQP4–IgG-positive Leigh syndrome: A case report and review of the literature
BACKGROUND: Leigh syndrome (LS; OMIM: 256000) is a progressive neurodegenerative disease caused by genetic mutations resulting in mitochondrial oxidative phosphorylation defects. The prognosis is poor, with most children dying before the age of 2 years. MT-ATP6 variants are the most common mitochond...
Autores principales: | Chen, Jun, Wang, Jianjun, Gan, Jing, Luo, Rong, Yang, Zuozhen, Liang, Mengmeng, Chen, Xiaolu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939766/ https://www.ncbi.nlm.nih.gov/pubmed/36814591 http://dx.doi.org/10.3389/fped.2023.1046731 |
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