Multifocal motor or sensory demyelinating mononeuropathy (Q92437): Difference between revisions
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A síndrome de Lewis-Sumner (SLS) é uma neuropatia sensitivo-motora desmielinizante multifocal autoimune. Deve ser considerada como uma variante clínica assimétrica da polineuropatia inflamatória desmielinizante crônica (PIDC). Os pacientes com SLS geralmente apresentam um envolvimento assimétrico do membro superior com déficit sensitivo-motor distal nos territórios mediano ou ulnar. | |||
| description / en | description / en | ||
Lewis- Sumner syndrome is a dysimmune multifocal demyelinating sensorimotor neuropathy. It should be considered as a clinical asymmetrical variant of chronic inflammatory demyelinating polyneuropathy (CIDP). Patients with LSS usually present with an asymmetrical involvement of the upper limb with distal sensorimotor deficit in median or ulnar territories. | |||
Revision as of 07:34, 16 August 2026
Lewis- Sumner syndrome is a dysimmune multifocal demyelinating sensorimotor neuropathy. It should be considered as a clinical asymmetrical variant of chronic inflammatory demyelinating polyneuropathy (CIDP). Patients with LSS usually present with an asymmetrical involvement of the upper limb with distal sensorimotor deficit in median or ulnar territories.
| Language | Label | Description | Also known as |
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| default for all languages | ID_980657399 |
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| English | Multifocal motor or sensory demyelinating mononeuropathy |
Lewis- Sumner syndrome is a dysimmune multifocal demyelinating sensorimotor neuropathy. It should be considered as a clinical asymmetrical variant of chronic inflammatory demyelinating polyneuropathy (CIDP). Patients with LSS usually present with an asymmetrical involvement of the upper limb with distal sensorimotor deficit in median or ulnar territories. |
