SPG11 and hereditary spastic paraplegia: The most common childhood onset HSP subtype in our cohort was SPG4, comprising 11/50 (22%) families with solved genetic diagnosis; followed by SPG3A, 8/50 families (16%); SPG11 in 5 families (10%) and SPG46 in 3 families with solved diagnosis and two families with bi-allelic candidate variants in GBA2 (Fig. 1A).