Motor neuron disease in hereditary spastic paraplegia (Q101501)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_349547398 |
||
| 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. |
Statements
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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