Motor neuron disease in dysproteinemia or gammopathy (Q101507): Difference between revisions
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A neuropatia motora raramente pode ser identificada em pacientes com gamopatia monoclonal. Pacientes com ELA têm uma taxa maior de gamopatia monoclonal e policlonal do que as populações de controle. | |||
| description / en | description / en | ||
Motor neuropathy may rarely be identified in patients with monoclonal gammopathy. Patients with ALS have a higher rate of monoclonal and polyclonal gammopathy than control populations. | |||
Revision as of 18:19, 16 August 2026
Motor neuropathy may rarely be identified in patients with monoclonal gammopathy. Patients with ALS have a higher rate of monoclonal and polyclonal gammopathy than control populations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_591825656 |
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| English | Motor neuron disease in dysproteinemia or gammopathy |
Motor neuropathy may rarely be identified in patients with monoclonal gammopathy. Patients with ALS have a higher rate of monoclonal and polyclonal gammopathy than control populations. |
