A case report of Leigh syndrome diagnosed by endomyocardial biopsy

BACKGROUND: Leigh syndrome is a neurodegenerative disorder caused by mitochondrial dysfunction with both phenotypic and genetic heterogeneity. Mitochondrial impairments are usually demonstrated by skeletal muscle biopsy. We report a case of Leigh syndrome diagnosed by endomyocardial biopsy (EMB), no...

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Detalles Bibliográficos
Autores principales: Maruo, Yuji, Ueda, Yuki, Murayama, Kei, Takeda, Atsuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898571/
https://www.ncbi.nlm.nih.gov/pubmed/33644659
http://dx.doi.org/10.1093/ehjcr/ytaa582

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898571/
https://www.ncbi.nlm.nih.gov/pubmed/33644659
http://dx.doi.org/10.1093/ehjcr/ytaa582

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