Autosomal recessive spastic paraplegia type 11

An autosomal recessive condition caused by mutation(s) in the SPG11 gene, encoding spatacsin. It is a complicated sub-type of hereditary spastic paraplegia that has varying neurologic manifestations in addition to spasticity.

Disease Alternative Name

spastic paraplegia
autosomal recessive
with thin corpus callosum
spastic paraplegia 11

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