Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions.
Carlos Estevez-FragaFrancesca MagrinelliDavina Hensman MossEoin MulroyGiulia Di LazzaroAnna LatorreMelissa MackenzieHenry HouldenSarah J TabriziKailash P BhatiaPublished in: Neurology. Genetics (2021)
MD are frequent in C9orf72. They may precede signs of ALS or FTD, or even be present in isolation. Parkinsonism, tremor, and myoclonus are most commonly observed.