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...
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| Main Authors: | , , , , |
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| Format: | article |
| Language: | EN |
| Published: |
University of São Paulo
2021
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| Subjects: | |
| Online Access: | https://doaj.org/article/4ac878d0d8df4c59ac2e5087a9fd4ca4 |
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