Hereditary spastic paraplegia 16

A hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2.

Also known as: SPG16, X-linked spastic paraplegia type 16, hereditary spastic paraplegia type 16, spastic paraplegia 16, X-linked, complicated, X-linked recessive, spastic paraplegia 16, spastic paraplegia 16, X-linked

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 16 itself.