Autosomal recessive spastic paraplegia type 14 (Q99406): Difference between revisions
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Latest revision as of 16:04, 16 August 2026
Autosomal recessive spastic paraplegia characterized by adulthood-onset of slowly progressive spastic paraplegia of lower limbs presenting with spastic gait, hyperreflexia, and mild lower limb hypertonicity associated with mild intellectual disability, visual agnosia, short and long-term memory deficiency, and mild distal motor neuropathy. Bilateral pes cavus and extensor plantar responses are also associated.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1304184567 |
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| English | Autosomal recessive spastic paraplegia type 14 |
Autosomal recessive spastic paraplegia characterized by adulthood-onset of slowly progressive spastic paraplegia of lower limbs presenting with spastic gait, hyperreflexia, and mild lower limb hypertonicity associated with mild intellectual disability, visual agnosia, short and long-term memory deficiency, and mild distal motor neuropathy. Bilateral pes cavus and extensor plantar responses are also associated. |
Statements
CID11:ID_1304184567
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dki-india-ID_1304184567
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Concluído
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15 August 2026
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