Adult-onset mitochondrial encephalopathy in association with the MT-ND3 T10158C mutation exhibits unique characteristics: A case report

BACKGROUND: Mitochondrial diseases are a heterogenous group of multisystemic disorders caused by genetic mutations affecting mitochondrial oxidation function. Brain involvement is commonly found in most cases but rarely as the unique clinical manifestation. Since the knowledge of its clinical manife...

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Detalles Bibliográficos
Autores principales: Fu, Xiao-Li, Zhou, Xiang-Xue, Shi, Zhu, Zheng, Wei-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511931/
https://www.ncbi.nlm.nih.gov/pubmed/31123680
http://dx.doi.org/10.12998/wjcc.v7.i9.1066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511931/
https://www.ncbi.nlm.nih.gov/pubmed/31123680
http://dx.doi.org/10.12998/wjcc.v7.i9.1066

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