Spinocerebellar Ataxia Type 27B (SCA27B): A Hereditary Ataxia in Portugal

Spinocerebellar ataxia type 27B (SCA27B) is a recently discovered hereditary disease caused by (GAA)≥250 repeat expansion in the fibroblast growth factor 14 (FGF14) gene, and multiple studies have recognized it as one of the most common causes of autosomal dominant ataxia in the European population. We present the case of a 62-year-old Portuguese patient who developed a slowly progressive gait impairment associated with wide-base ataxic gait, dysarthria, left upper limb dysmetria, and dysdiadochokinesia. This pure cerebellar phenotype had an episodic worsening induced by intense physical activity and alcohol intake. The patient had an older brother with a late-onset cerebellar ataxia of unknown cause. Genetic testing detected a heterozygotic intronic FGF14 repeat expansion with complete penetrance (> 360 repeats), confirming the diagnosis of SCA27B. To our knowledge, we present the first reported case of SCA27B in the Portuguese population.

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Journal
Acta Médica Portuguesa
Published
2024-10-11
DOI
https://doi.org/10.20344/amp.22232
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1
Primary Topic
Genetic Neurodegenerative Diseases
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article
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0.27
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article

Spinocerebellar Ataxia Type 27B (SCA27B): A Hereditary Ataxia in Portugal

Raquel Barbosa, Marta Magriço, Bruna Meira, Vítor Mendes Ferreira
1 citations
Acta Médica Portuguesa
Genetic Neurodegenerative Diseases
0.27
article

Spinocerebellar Ataxia Type 27B (SCA27B): A Hereditary Ataxia in Portugal

Raquel Barbosa, Marta Magriço, Bruna Meira, Vítor Mendes Ferreira
article en
1 citations

Abstract

Spinocerebellar ataxia type 27B (SCA27B) is a recently discovered hereditary disease caused by (GAA)≥250 repeat expansion in the fibroblast growth factor 14 (FGF14) gene, and multiple studies have recognized it as one of the most common causes of autosomal dominant ataxia in the European population. We present the case of a 62-year-old Portuguese patient who developed a slowly progressive gait impairment associated with wide-base ataxic gait, dysarthria, left upper limb dysmetria, and dysdiadochokinesia. This pure cerebellar phenotype had an episodic worsening induced by intense physical activity and alcohol intake. The patient had an older brother with a late-onset cerebellar ataxia of unknown cause. Genetic testing detected a heterozygotic intronic FGF14 repeat expansion with complete penetrance (> 360 repeats), confirming the diagnosis of SCA27B. To our knowledge, we present the first reported case of SCA27B in the Portuguese population.

Acta Médica PortuguesaVol. 38(6-7)
Centre Hospitalier Universitaire de Toulouse (FR), Hospital de Egas Moniz (PT)
Good health and well-being
Openalex Percentile: Top 44%
Genetic Neurodegenerative Diseases
0.27
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Spinocerebellar Ataxia Type 27B (SCA27B): A Hereditary Ataxia in Portugal — Raquel Barbosa, Marta Magriço, et al. · Acta Médica Portuguesa (2024) | TGRS Research Map | TGRS