An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions

BACKGROUND: The detailed neuropathological features of patients with autosomal recessive hereditary spastic paraplegia with a thin corpus callosum (TCC) and SPG11 mutations are poorly understood, as only a few autopsies have been reported. Herein, we describe the clinicopathological findings of a pa...

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Detalles Bibliográficos
Autores principales: Hayakawa, Mika, Matsubara, Tomoyasu, Mochizuki, Yoko, Takeuchi, Chisen, Minamitani, Motoyuki, Imai, Masayuki, Kosaki, Kenjiro, Arai, Tomio, Murayama, Shigeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722294/
https://www.ncbi.nlm.nih.gov/pubmed/34979968
http://dx.doi.org/10.1186/s12883-021-02514-z

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