Autosomal dominant spastic paraplegia type 6 (Q100874)
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Autosomal dominant spastic paraplegia that usually presents in late adolescence or early adulthood as a pure phenotype of lower limb spasticity with hyperreflexia and extensor plantar responses, as well as mild bladder disturbances and pes cavus. Rarely, it can present as a complex phenotype with additional manifestations including epilepsy, variable peripheral neuropathy and/or memory impairment.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_434114972 |
||
| English | Autosomal dominant spastic paraplegia type 6 |
Autosomal dominant spastic paraplegia that usually presents in late adolescence or early adulthood as a pure phenotype of lower limb spasticity with hyperreflexia and extensor plantar responses, as well as mild bladder disturbances and pes cavus. Rarely, it can present as a complex phenotype with additional manifestations including epilepsy, variable peripheral neuropathy and/or memory impairment. |
Statements
CID11:ID_434114972
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dki-india-ID_434114972
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Concluído
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15 August 2026
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