Autoimmune sensory ganglionopathy (Q85115)

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Autoimmune sensory ganglionopathy occurs as acute sensory neuropathy, in association with Sjögren`s syndrome also pansensory, small fibre, CANVAS (Cerebellar Ataxia, neuropathy, vestibular areflexia syndrome, toxic conditions as pyridoxin intoxication and also cis platinum treatment must be considered. It has a subacute onset, severe sensory loss resulting in ataxia. The onset can be asymmetric, often beginning in the arms and associated with neuropathic pain. Once established it has a chronic and unremitting course disabling the patient.
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ID_167268801
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    Autoimmune sensory ganglionopathy
    Autoimmune sensory ganglionopathy occurs as acute sensory neuropathy, in association with Sjögren`s syndrome also pansensory, small fibre, CANVAS (Cerebellar Ataxia, neuropathy, vestibular areflexia syndrome, toxic conditions as pyridoxin intoxication and also cis platinum treatment must be considered. It has a subacute onset, severe sensory loss resulting in ataxia. The onset can be asymmetric, often beginning in the arms and associated with neuropathic pain. Once established it has a chronic and unremitting course disabling the patient.

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      CID11:ID_167268801
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      dki-india-ID_167268801
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      Concluído
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      13 August 2026
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