Hereditary spastic paraplegia 17

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the BSCL2 gene.

Also known as: BSCL2 hereditary spastic paraplegia, SPG17, Silver spastic paraplegia syndrome, Silver syndrome, autosomal dominant spastic paraplegia type 17, hereditary spastic paraplegia caused by mutation in BSCL2, hereditary spastic paraplegia type 17, spastic paraplegia with amyotrophy of hands and feet

15 clinical trials for this condition and its sub-types.