Autosomal dominant spastic paraplegia type 37 (Q100920): Difference between revisions
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Forma de paraplegia espástica hereditária caracterizada por início entre a infância e a idade adulta de marcha espástica lentamente progressiva, respostas extensoras plantares, reflexos tendinosos enérgicos nos braços e pernas, diminuição da sensação de vibração e disfunção urinária. | |||
| description / en | description / en | ||
A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction. | |||
Revision as of 17:42, 16 August 2026
A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1636862745 |
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| English | Autosomal dominant spastic paraplegia type 37 |
A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction. |
