Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary spastic paraplegia · KIF5A-related neurological disorder
Hereditary spastic paraplegia 10
Autosomal dominant spastic paraplegia type 10 (SPG10) is a rare type of hereditary spastic paraplegia that can present as either a pure form of spastic paraplegia with lower limb spasticity, hyperreflexia and extensor plantar responses, presenting in childhood or adolescence, or as a complex phenotype associated with additional manifestations including peripheral neuropathy with upper limb amyotrophy, moderate intellectual disability and parkinsonism. Deafness and retinitis pigmentosa were reported in one case.
This condition has no sub-types.