Natural history of motor neuron disease in adult onset GM2-gangliosidosis: A case report with 25 years of follow-up

An adult with Sandhoff disease presented with pure lower motor neuron phenotype. Twenty years later, he showed signs of upper motor neuron involvement. 25 years from the onset, his muscle weakness slightly worsened but he was fully independent in activities of daily living. GM2-gangliosidosis can ma...

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Detalles Bibliográficos
Autores principales: Scarpelli, Mauro, Tomelleri, Giuliano, Bertolasi, Laura, Salviati, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121317/
https://www.ncbi.nlm.nih.gov/pubmed/27896099
http://dx.doi.org/10.1016/j.ymgmr.2014.06.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121317/
https://www.ncbi.nlm.nih.gov/pubmed/27896099
http://dx.doi.org/10.1016/j.ymgmr.2014.06.002

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