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: | Book |
| Published: |
University of São Paulo,
2021-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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