Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5
oleh: Romina Romaniello, Andrea Citterio, Elena Panzeri, Filippo Arrigoni, Marta De Rinaldis, Antonio Trabacca, Maria Teresa Bassi
| Format: | Article |
|---|---|
| Diterbitkan: | Wiley 2021-04-01 |
Deskripsi
Abstract In the present study, we describe two novel cases of SCA5 with early onset. The first one, carrying a novel heterozygous de novo missense mutation in SPTBN2 gene, showed a striking very severe cerebellar atrophy and reduction of volume of the pons at a very young age (16 months). The latter, carrying the first de novo intragenic deletion so far reported in SPTBN2 gene, showed a mild cerebellar atrophy involving the hemispheres and a later onset. In both cases, for the first time, a hyperintense signal of the dentate nuclei was observed.