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Article

Gait disorders in fatal familial insomnia.

Movement disorders : official journal of the Movement Disorder Society - 1 Mar 2014

Cortelli Pietro, Fabbri Margherita, Calandra-Buonaura Giovanna, Capellari Sabina, Tinuper Paolo, Parchi Piero, Lugaresi Elio

Abstract excerpt

BACKGROUND: 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 d...

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Identifiers

PMID: 24375448
DOI: 10.1002/mds.25786

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24375448-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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