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Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation

✍ Scribed by Romagnolo, A.; Masera, S.; Mattioda, A.; Superti, G.; Santorelli, F. M.; Mongini, T.; Pinessi, L.; Cavalla, P.


Book ID
124090882
Publisher
John Wiley and Sons
Year
2014
Tongue
English
Weight
462 KB
Volume
21
Category
Article
ISSN
1351-5101

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## Abstract **Background:** Autosomal recessive hereditary spastic paraplegia with thin corpus callosum is a neurodegenerative disorder characterized by spastic paraparesis, cognitive impairment, and peripheral neuropathy. The neuroradiologic hallmarks are thin corpus callosum and periventricular w