Prevalence of FGF14-mediated Spinocerebellar Ataxia 27B (SCA27B) in a United States Cohort (P6-5.015)

Repeat expansions in the FGF14 gene cause spinocerebellar ataxia 27B (SCA27B), a slowly progressive adult-onset cerebellar ataxia. This may be a common genetic cause of adult-onset ataxia, with cohort studies suggesting diagnostic rates of between 10–61% in various populations worldwide, however, prevalence studies have yet to be performed in the United States.

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Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000210524
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Prevalence of FGF14-mediated Spinocerebellar Ataxia 27B (SCA27B) in a United States Cohort (P6-5.015)

Brent L. Fogel, Sonya Watson, Anirudh N. Eranki, Hannah Stevens et al.
1 links
Neurology
Genetic Neurodegenerative Diseases
article

Prevalence of FGF14-mediated Spinocerebellar Ataxia 27B (SCA27B) in a United States Cohort (P6-5.015)

Brent L. Fogel, Sonya Watson, Anirudh N. Eranki, Hannah Stevens, Darice Y. Wong, Veronica S. Avila
article en

Abstract

Repeat expansions in the FGF14 gene cause spinocerebellar ataxia 27B (SCA27B), a slowly progressive adult-onset cerebellar ataxia. This may be a common genetic cause of adult-onset ataxia, with cohort studies suggesting diagnostic rates of between 10–61% in various populations worldwide, however, prevalence studies have yet to be performed in the United States.

NeurologyVol. 104(7_Supplement_1)
UCLA Health (US)
Openalex Percentile: Top 92%
Genetic Neurodegenerative Diseases
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