Motor neuron disease in autoimmune disease including increased anti-GMl ganglioside antibody (Q101489): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank

Revision as of 18:18, 16 August 2026

There is a higher incidence of motor neuron disease (MND) in patients with preceding autoimmune disease, suggesting possible shared genetic or environmental risk factors. Occasional reports have documented the coexistence of MND with symptomatic autoimmune disease. Multifocal motor neuropathy (MMN), a mimic of MND, may be associated with anti GM1 ganglioside antibodies. Low-titre anti-GM1 ganglioside antibodies may be detected in patients with MND, without clinical or neurophysiological features of MMN.
Language Label Description Also known as
default for all languages
ID_955868778
    English
    Motor neuron disease in autoimmune disease including increased anti-GMl ganglioside antibody
    There is a higher incidence of motor neuron disease (MND) in patients with preceding autoimmune disease, suggesting possible shared genetic or environmental risk factors. Occasional reports have documented the coexistence of MND with symptomatic autoimmune disease. Multifocal motor neuropathy (MMN), a mimic of MND, may be associated with anti GM1 ganglioside antibodies. Low-titre anti-GM1 ganglioside antibodies may be detected in patients with MND, without clinical or neurophysiological features of MMN.

      Statements

      CID11:ID_955868778
      0 references
      dki-india-ID_955868778
      0 references
      Concluído
      0 references