Motor neuron disease in hereditary spastic paraplegia (Q101501): Difference between revisions
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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 |
|---|---|---|---|
| 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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