Autosomal dominant spastic paraplegia type 8 (Q100885): Difference between revisions

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Latest revision as of 17:39, 16 August 2026

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.

Language	Label	Description	Also known as
default for all languages	ID_779301090
English	Autosomal dominant spastic paraplegia type 8	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.