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- 2018
Dystonia in Patients with Spinocerebellar Ataxia 3 - Machado-Joseph disease: An Underestimated Diagnosis?DOI: 10.2174/1874205X01812010041 Keywords: Dystonia, Machado-Joseph disease, Spinocerebellar ataxias, Genetic epidemiology, Movement disorders Abstract: Spinocerebellar Ataxia type 3 (SCA3) or Machado-Joseph Disease (MJD) is characterized by cerebellar, central and peripheral symptoms, including movement disorders. Dystonia can be classified as hereditary and neurodegenerative when present in SCA3
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