Catalog

Autosomal dominant spastic paraplegia type 8

No MMS code

Link to WHO Definition

Autosomal dominant spastic paraplegia type 8 – http://id.who.int/icd/entity/779301090

Autosomal dominant pure hereditary spastic paraplegia characterized by early to mid-adulthood onset of slowly progressive lower limb spasticity resulting in gait disturbances, hyperreflexia and extensor plantar responses, that may be associated with complicating signs, such as upper limb involvement, sensory neuropathy, ataxia, and mild dysphagia.