X-linked spastic paraplegia type 2 (Q97741): Difference between revisions
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Paraplegia espástica tipo 2 (SPG2) é uma leucodistrofia ligada ao X caracterizada primariamente por marcha espástica e disfunção autonômica. Quando outros sinais do sistema nervoso central (SNC), como déficit intelectual, ataxia ou sinais extrapiramidais, estão presentes, a síndrome é chamada de SPG2 complicado. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Spastic paraplegia type 2 (SPG2) is an X-linked leukodystrophy characterised primarily by spastic gait and autonomic dysfunction. When additional central nervous system (CNS) signs, such as intellectual deficit, ataxia, or extrapyramidal signs, are present, the syndrome is referred to as complicated SPG2. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1847361827 / rank | |||||||||||||||
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CID11:ID_1847361827 | |||||||||||||||
| Property / CURIE: CID11:ID_1847361827 / rank | |||||||||||||||
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dki-india-ID_1847361827 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1847361827 / 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 13:52, 16 August 2026
Spastic paraplegia type 2 (SPG2) is an X-linked leukodystrophy characterised primarily by spastic gait and autonomic dysfunction. When additional central nervous system (CNS) signs, such as intellectual deficit, ataxia, or extrapyramidal signs, are present, the syndrome is referred to as complicated SPG2.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1847361827 |
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| English | X-linked spastic paraplegia type 2 |
Spastic paraplegia type 2 (SPG2) is an X-linked leukodystrophy characterised primarily by spastic gait and autonomic dysfunction. When additional central nervous system (CNS) signs, such as intellectual deficit, ataxia, or extrapyramidal signs, are present, the syndrome is referred to as complicated SPG2. |
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CID11:ID_1847361827
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dki-india-ID_1847361827
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Concluído
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15 August 2026
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