Leigh syndrome in an infant: autopsy and histopathology findings

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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Bibliographic Details
Main Authors: Arushi Gahlot Saini, Debjyoti Chatterjee, Chandana Bhagwat, Sameer Vyas, Savita Verma Attri
Format: Article
Language:English
Published: University of São Paulo 2021-11-01
Series:Autopsy and Case Reports
Subjects:
Basal Ganglia
Brain Damage
Chronic
Leigh Disease
Mitochondrial Diseases
Online Access:https://www.revistas.usp.br/autopsy/article/view/192669

Internet

https://www.revistas.usp.br/autopsy/article/view/192669

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