Article

Middle childhood onset Spinocerebellar Ataxia Type 2

2023-08-25

Abstract excerpt

Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant ataxia characterized by progressive cerebellar ataxia, slow saccades, pyramidal findings and parkinsonism, caused by triplet CAG expansion in the ATXN2 gene in chromosome 12. Age of onset is typically in the fourth decade with 10- to 15-year disease duration. We present a case of SCA2 with symptom onset within the first decade of life with extrapyramida...

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Literature Corpus work: 2874c618-5a02-5b1d-a512-a0b38aac5cc5
DOI: 10.22541/au.169294456.61234531/v1

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