04.04.2024 | Letter to the Editor
Adult-onset spastic paraplegia associated with a novel SPTBN2 missense heterozygous variant
verfasst von:
Francesca Palumbo, Antonio Canosa, Cristina Moglia, Andrea Calvo, Salvatore Gallone
Erschienen in:
Acta Neurologica Belgica
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Excerpt
Hereditary spastic paraplegia (HSP) encompasses a heterogeneous group of neurodegenerative disorders affecting corticospinal tracts, leading to a progressive lower limbs pyramidal syndrome [
1]. The introduction of next-generation (NGS) sequencing has extended the genetic underpinnings of HSP, revealing a molecular overlap between HSP and ataxic syndromes situated at opposite ends of a disease continuum [
2]. Mutations in the spectrin beta non-erythrocytic 2 (SPTBN2) gene have been linked to spinocerebellar ataxia type (SCA) 5 and SCA14 [
3]. Herein, we present the first case of pure spastic paraplegia associated with a novel missense heterozygous variant in the SPTBN2 gene. …