Motor neuron disease in hereditary spastic paraplegia (Q101501): Difference between revisions
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Em alguns subtipos genéticos de paraplegia espástica hereditária, os pacientes demonstram sinais clínicos ou evidências neurofisiológicas de neuropatia sensitivo-motora ou, mais raramente, neuropatia motora pura. Isso pode dificultar a diferenciação de ELA. | |||||||||||||||
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In some genetic subtypes of hereditary spastic paraplegia, patients demonstrate clinical signs or neurophysiological evidence of sensorimotor, or more rarely, pure motor neuropathy. This may make differentiation from ALS difficult. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/349547398 / rank | |||||||||||||||
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CID11:ID_349547398 | |||||||||||||||
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dki-india-ID_349547398 | |||||||||||||||
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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 18:19, 16 August 2026
In some genetic subtypes of hereditary spastic paraplegia, patients demonstrate clinical signs or neurophysiological evidence of sensorimotor, or more rarely, pure motor neuropathy. This may make differentiation from ALS difficult.
| Language | Label | Description | Also known as |
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| default for all languages | ID_349547398 |
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| English | Motor neuron disease in hereditary spastic paraplegia |
In some genetic subtypes of hereditary spastic paraplegia, patients demonstrate clinical signs or neurophysiological evidence of sensorimotor, or more rarely, pure motor neuropathy. This may make differentiation from ALS difficult. |
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CID11:ID_349547398
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dki-india-ID_349547398
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Concluído
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15 August 2026
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