Autosomal dominant spastic paraplegia type 8 (Q100885): Difference between revisions
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Paraplegia espástica hereditária pura autossômica dominante, caracterizada por início precoce a meados da idade adulta de espasticidade lentamente progressiva de membros inferiores, resultando em distúrbios da marcha, hiperreflexia e respostas extensoras plantares, que podem estar associadas a sinais complicadores, como envolvimento dos membros superiores, neuropatia sensorial, ataxia, e disfagia leve. | |||
| description / en | description / en | ||
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. | |||
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 |
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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. |
