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 / endescription / 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.
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Property / Canonical URI: https://id.who.int/icd/entity/803014219 / rank
 
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CID11:ID_803014219
Property / CURIE: CID11:ID_803014219 / rank
 
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dki-india-ID_803014219
Property / Canary Token: dki-india-ID_803014219 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
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Latest 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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ID_803014219
    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.

      Statements

      CID11:ID_803014219
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      dki-india-ID_803014219
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      Concluído
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      15 August 2026
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