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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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| Yayımlandı: | Eur Heart J Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7898571/ https://ncbi.nlm.nih.gov/pubmed/33644659 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ehjcr/ytaa582 |
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