Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5

Abstract In the present study, we describe two novel cases of SCA5 katin mens shirts 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 corgi pup knife 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.