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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Detalles Bibliográficos
Autores principales: Saini, Arushi Gahlot, Chatterjee, Debjyoti, Bhagwat, Chandana, Vyas, Sameer, Attri, Savita Verma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital Universitário da Universidade de São Paulo 2021
Materias:
Autopsy Case Report
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

Internet

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

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