Autosomal recessive spastic paraplegia type 14 (Q99406): Difference between revisions
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Paraplegia espástica autossômica recessiva caracterizada por paraplegia espástica lentamente progressiva de membros inferiores, com início na idade adulta, apresentando marcha espástica, hiperreflexia e hipertonicidade leve de membros inferiores associada a incapacidade intelectual leve, agnosia visual, deficiência de memória de curto e longo prazo e neuropatia motor distal leve. Pés cavos bilaterais e respostas extensoras plantares também estão associadas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1304184567 / rank | |||||||||||||||
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CID11:ID_1304184567 | |||||||||||||||
| Property / CURIE: CID11:ID_1304184567 / rank | |||||||||||||||
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dki-india-ID_1304184567 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1304184567 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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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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