%0 Journal Article
%T Dystonia in Patients with Spinocerebellar Ataxia 3 - Machado-Joseph disease: An Underestimated Diagnosis?
%A Adriana Moro
%A Carlos Henrique Ferreira Camargo
%A Gustavo Ribas
%A H¨Ślio Afonso Ghizoni Teive
%A Ligia Maria Perrucci Catai
%A Salmo Raskin
%J Archive of "The Open Neurology Journal".
%D 2018
%R 10.2174/1874205X01812010041
%X 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
%K Dystonia
%K Machado-Joseph disease
%K Spinocerebellar ataxias
%K Genetic epidemiology
%K Movement disorders
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008980/