Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation

Patients with TARDBP mutations have so far been classified as ALS, sometimes with frontal lobe dysfunction. A 66-year-old patient progressively developed a severe sensory disorder, followed by a motor disorder, which evolved over nine years. Symptoms started in the left hand and slowly involved the...

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Detalles Bibliográficos
Autores principales: Camdessanché, Jean-Philippe, Belzil, Véronique V, Jousserand, Guillemette, Rouleau, Guy A, Créac'h, Christelle, Convers, Philippe, Antoine, Jean-Christophe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042904/
https://www.ncbi.nlm.nih.gov/pubmed/21294910
http://dx.doi.org/10.1186/1750-1172-6-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042904/
https://www.ncbi.nlm.nih.gov/pubmed/21294910
http://dx.doi.org/10.1186/1750-1172-6-4

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