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Leigh syndrome in an infant: autopsy and histopathology findings
Leigh syndrome is an inherited neurodegenerative disorder of infancy that typically manifests between 3 and 12 months of age. The common neurological manifestations are developmental delay or regression, progressive cognitive decline, dystonia, ataxia, brainstem dysfunction, epileptic seizures, and...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Hospital Universitário da Universidade de São Paulo
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597803/ https://www.ncbi.nlm.nih.gov/pubmed/34805005 http://dx.doi.org/10.4322/acr.2021.334 |