Three Cases of Spinocerebellar Ataxia Type 2 (SCA2) and Pediatric Literature Review: Do Not Forget Trinucleotide Repeat Disorders in Childhood-Onset Progressive Ataxia

<b>Background</b>: Childhood-onset progressive ataxias are rare neurodegenerative disorders characterized by cerebellar signs, sometimes associated with other neurological or extra-neurological features. The autosomal dominant forms, known as spinocerebellar ataxias (SCAs), linked to trinucleotide (...

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Detalhes bibliográficos

Principais autores:	Jacopo Sartorelli, Maria Grazia Pomponi, Giacomo Garone, Gessica Vasco, Francesca Cumbo, Vito Luigi Colona, Adele D’Amico, Enrico Bertini, Francesco Nicita
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2025-02-01
Colecção:	Brain Sciences
Assuntos:	spinocerebellar ataxias movement disorder pediatric CAG myoclonus SCA
Acesso em linha:	https://www.mdpi.com/2076-3425/15/2/156
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