Abstract
Around 10% of all amyotrophic lateral sclerosis (ALS) cases are familial and around 3–5% are fused-in-sarcoma (FUS)-related in Europe. We report a 43-year-old patient with a pathogenic FUS mutation (c.1561C>G p.(Arg521Gly) who presented at our clinic with chorea and subsequently with progressive symptoms of classical ALS. As a result of progressive upper and lower motor neurone deterioration, chorea disappeared and death occurred 2.5 years after the onset of the first manifestations. This first description adds chorea as a possible pleiotropic clinical feature in FUS-related ALS. It further warrants to systematically ask and check for chorea in ALS patients and their relatives.
Original language | English |
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Pages (from-to) | 309-311 |
Number of pages | 3 |
Journal | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration |
Volume | 21 |
Issue number | 3-4 |
DOIs | |
Publication status | Published - May 2020 |
Keywords
- Amyotrophic lateral sclerosis
- chorea
- fused-in-sarcoma