Polyneuropathy in Patients with Spinocerebellar Ataxias Types 2, 3, and 10: A Systematic Review

Spinocerebellar ataxia (SCA) is an autosomal dominant hereditary disease with a low prevalence, for which more than 50 types have been described. This group of neurodegenerative diseases can present as different phenotypes with varying progression rates and clinical manifestations of different sever...

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Veröffentlicht in:	Cerebellum (London, England) England), 2024-12, Vol.23 (6), p.2593-2606
Hauptverfasser:	de Almeida Franzoi, André Eduardo, da Silva, Gustavo Figueiredo, de Souza Somensi, Eduardo, de Moura Campos, Marcelo Henrique, Wollmann, Giulia Murillo, Fustes, Otto Jesus Hernandez, Marques, Gustavo Lenci, Teive, Helio Afonso Ghizoni
Format:	Artikel
Sprache:	eng
Schlagworte:	Biomedical and Life Sciences Biomedicine Hereditary diseases Machado-Joseph disease Neurobiology Neurodegenerative diseases Neurology Neurosciences Patients Peripheral neuropathy Phenotypes Polyglutamine Polyneuropathy Review Spinocerebellar ataxia Trinucleotide repeats
Online-Zugang:	Volltext
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