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...

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Detalles Bibliográficos
Autores principales: Chen, Jun, Wang, Jianjun, Gan, Jing, Luo, Rong, Yang, Zuozhen, Liang, Mengmeng, Chen, Xiaolu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
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

Internet

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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