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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Auteurs principaux: Arushi Gahlot Saini, Debjyoti Chatterjee, Chandana Bhagwat, Sameer Vyas, Savita Verma Attri
Format: article
Langue:EN
Publié: University of São Paulo 2021
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R
Accès en ligne:https://doaj.org/article/4ac878d0d8df4c59ac2e5087a9fd4ca4
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