Chorea is a pleiotropic clinical feature of mutated fused-in-sarcoma in amyotrophic lateral sclerosis
Publication date
2020-05
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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.
Keywords
Amyotrophic lateral sclerosis, chorea, fused-in-sarcoma, Clinical Neurology, Neurology, Journal Article
Citation
Flies, C M & Veldink, J H 2020, 'Chorea is a pleiotropic clinical feature of mutated fused-in-sarcoma in amyotrophic lateral sclerosis', Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol. 21, no. 3-4, pp. 309-311. https://doi.org/10.1080/21678421.2020.1733021