Autosomal dominant spastic paraplegia type 37 (Q100920): Difference between revisions
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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. |
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CID11:ID_1636862745
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