Autosomal dominant spastic paraplegia type 8 (Q100885): Difference between revisions
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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 |
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| default for all languages | ID_779301090 |
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| 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. |
