Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2
- PMID: 12705795
- DOI: 10.2169/internalmedicine.42.277
Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2
Abstract
We report a case of amyotrophic lateral sclerosis (ALS) with IgM antibody against gangliosides GM2 and GD2. A 57-year-old woman presented with slowly progressive muscular weakness of the upper extremities and dysarthria. She fulfilled the clinical and electrophysiological criteria of ALS, and died from sudden suffocation about 3 years after the onset of illness. The patient's serum IgM antibody was shown to recognize the structure shared by GM2 and GD2. Since anti-GM2 antibodies have been implicated in motor neuropathy or motor neuron syndrome, this rare case might contribute to the understanding of the immunological aspects of ALS.
Comment in
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Antibodies to GM2 ganglioside in neurological disorders.Intern Med. 2003 Mar;42(3):220-1. doi: 10.2169/internalmedicine.42.220. Intern Med. 2003. PMID: 12705785 No abstract available.
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