CANOMAD - [Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies] syndrome (Q92430): Difference between revisions
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A síndrome CANOMAD (neuropatia atáxica crônica, oftalmoplegia, proteína IgM monoclonal, aglutininas frias e anticorpos Disialosil) é uma polineuropatia desmielinizante imunomediada crônica rara com ataxia sensorial acentuada e arreflexia, e com função motora relativamente preservada nos membros. | |||
| description / en | description / en | ||
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. | |||
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.
| Language | Label | Description | Also known as |
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| default for all languages | ID_803014219 |
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| English | 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. |
