Dystonia in Patients with Spinocerebellar Ataxia 3 - Machado-Joseph disease: An Underestimated Diagnosis?

BACKGROUND: 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. OBJECTIVE: The objective of this study...

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Publicat a:Open Neurol J
Autors principals: Catai, Ligia Maria Perrucci, Camargo, Carlos Henrique Ferreira, Moro, Adriana, Ribas, Gustavo, Raskin, Salmo, Teive, Hélio Afonso Ghizoni
Format: Artigo
Idioma:Inglês
Publicat: Bentham Open 2018
Matèries:
Neurology
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6008980/
https://ncbi.nlm.nih.gov/pubmed/30008965
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1874205X01812010041
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