CANOMAD - [Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies] syndrome (Q92430): Difference between revisions

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Revision as of 07:34, 16 August 2026

CANOMAD syndrome (Chronic Ataxic Neuropathy, Ophthalmoplegia, Monoclonal IgM protein, cold Agglutinins and Disialosyl antibodies) is a rare chronic immune-mediated demyelinating polyneuropathy with marked sensory ataxia and areflexia, and with relatively preserved motor function in the limbs.
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    CANOMAD - [Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies] syndrome
    CANOMAD syndrome (Chronic Ataxic Neuropathy, Ophthalmoplegia, Monoclonal IgM protein, cold Agglutinins and Disialosyl antibodies) is a rare chronic immune-mediated demyelinating polyneuropathy with marked sensory ataxia and areflexia, and with relatively preserved motor function in the limbs.

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