Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Pure hereditary spastic paraplegia
Hereditary spastic paraplegia 12
Autosomal dominant spastic paraplegia type 12 is a pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.
This condition has no sub-types.