Late-Onset Spinocerebellar Ataxia 2 with Only 32 CAG Repeats

Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder caused by CAG trinucleotide repeat expansion in the ATXN2 gene. Only a few SCA2 patients with intermediate alleles (32-34 repeats) have been reported. Herein, we describe a patient confirmed to have SCA2 with 32 CAG repeats in ATXN2. A 66-year-old man presented with progressive unsteadiness and dysarthria for several months. Brain magnetic resonance imaging (MRI) showed diffuse cerebellar atrophy, and genetic analysis confirmed 32/22 CAG repeats in ATXN2. CAG repeat counts in ATXN2 are typically approximately 22 in 90% of the general population, with very low polymorphism. These findings suggest that even a minimal expansion beyond the normal upper limit may be sufficient to cause disease, albeit with a markedly delayed onset.

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Publication Details

Journal
Journal of the Korean Neurological Association
Published
2026-07-30
DOI
https://doi.org/10.17340/jkna.2026.0003
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
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article

Late-Onset Spinocerebellar Ataxia 2 with Only 32 CAG Repeats

Yun Jeong Hong, Seonghoon Kim, Taewon Kim, S Y Na
Journal of the Korean Neurological Association
Genetic Neurodegenerative Diseases
article

Late-Onset Spinocerebellar Ataxia 2 with Only 32 CAG Repeats

Yun Jeong Hong, Seonghoon Kim, Taewon Kim, S Y Na
article en

Abstract

Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder caused by CAG trinucleotide repeat expansion in the ATXN2 gene. Only a few SCA2 patients with intermediate alleles (32-34 repeats) have been reported. Herein, we describe a patient confirmed to have SCA2 with 32 CAG repeats in ATXN2. A 66-year-old man presented with progressive unsteadiness and dysarthria for several months. Brain magnetic resonance imaging (MRI) showed diffuse cerebellar atrophy, and genetic analysis confirmed 32/22 CAG repeats in ATXN2. CAG repeat counts in ATXN2 are typically approximately 22 in 90% of the general population, with very low polymorphism. These findings suggest that even a minimal expansion beyond the normal upper limit may be sufficient to cause disease, albeit with a markedly delayed onset.

Journal of the Korean Neurological AssociationVol. 44(3)
The Catholic University of Korea Incheon St. Mary's Hospital (KR), The Catholic University of Korea Uijeongbu St. Mary's Hospital (KR), Catholic University of Korea (KR)
Good health and well-being
Openalex Percentile: Top 14%
Genetic Neurodegenerative Diseases
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