Autoimmune sensory ganglionopathy, neural autoantibody positive (Q101018): Difference between revisions
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Revision as of 17:48, 16 August 2026
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. Antibody positive: Antibody profiles are currently unknown.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1275925881 |
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| English | Autoimmune sensory ganglionopathy, neural autoantibody positive |
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. Antibody positive: Antibody profiles are currently unknown. |
