Fatal familial insomnia (FFI) is a hereditary autosomal-dominant prion disease linked to a mutation of the prion protein gene and characterized by sleep and autonomic abnormalities at onset followed by motor disturbances. We describe gait abnormalities in 13 FFI cases with different disease durations.
Cortelli, P., Fabbri, M., Calandra-Buonaura, G., Capellari, S., Tinuper, P., Parchi, P., et al. (2014). Gait disorders in fatal familial insomnia. MOVEMENT DISORDERS, 29(3), 420-424 [10.1002/mds.25786].
Gait disorders in fatal familial insomnia
CORTELLI, PIETRO;CALANDRA BUONAURA, GIOVANNA;CAPELLARI, SABINA;TINUPER, PAOLO;PARCHI, PIERO;
2014
Abstract
Fatal familial insomnia (FFI) is a hereditary autosomal-dominant prion disease linked to a mutation of the prion protein gene and characterized by sleep and autonomic abnormalities at onset followed by motor disturbances. We describe gait abnormalities in 13 FFI cases with different disease durations.File in questo prodotto:
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