FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

BACKGROUND: Frontotemporal lobar degeneration with ubiquitin and TDP-43 positive neuronal inclusions represents a novel entity (FTLD-TDP) that may be associated with motor neuron disease (FTLD-MND); involvement of extrapyramidal and other systems has also been reported. CASE PRESENTATION: We present...

Descripción completa

Detalles Bibliográficos
Autores principales: Rusina, Robert, Kovacs, Gabor G, Fiala, Jindřich, Hort, Jakub, Ridzoň, Petr, Holmerová, Iva, Ströbel, Thomas, Matěj, Radoslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112085/
https://www.ncbi.nlm.nih.gov/pubmed/21569259
http://dx.doi.org/10.1186/1471-2377-11-50

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112085/
https://www.ncbi.nlm.nih.gov/pubmed/21569259
http://dx.doi.org/10.1186/1471-2377-11-50

Ejemplares similares