Autosomal recessive spastic paraplegia type 27 (Q99395): Difference between revisions
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Paraplegia espástica hereditária caracterizada por início variável de espasticidade lentamente progressiva de membros inferiores, hiperreflexia e respostas extensoras plantares, que podem estar associadas a polineuropatia sensório-motora, diminuição da sensação de vibração, consumpção muscular distal dos membros inferiores, disartria e incapacidade intelectual leve a moderada. | |||
| description / en | description / en | ||
Hereditary spastic paraplegia characterized by variable onset of slowly progressive lower limb spasticity, hyperreflexia and extensor plantar responses, that may be associated with sensorimotor polyneuropathy, decreased vibration sense, lower limb distal muscle wasting, dysarthria and mild to moderate intellectual disability. | |||
Revision as of 16:03, 16 August 2026
Hereditary spastic paraplegia characterized by variable onset of slowly progressive lower limb spasticity, hyperreflexia and extensor plantar responses, that may be associated with sensorimotor polyneuropathy, decreased vibration sense, lower limb distal muscle wasting, dysarthria and mild to moderate intellectual disability.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2071907645 |
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| English | Autosomal recessive spastic paraplegia type 27 |
Hereditary spastic paraplegia characterized by variable onset of slowly progressive lower limb spasticity, hyperreflexia and extensor plantar responses, that may be associated with sensorimotor polyneuropathy, decreased vibration sense, lower limb distal muscle wasting, dysarthria and mild to moderate intellectual disability. |
