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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...
Autores principales: | Scarpelli, Mauro, Tomelleri, Giuliano, Bertolasi, Laura, Salviati, Alessandro |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
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 |
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