Autoimmune sensory ganglionopathy, neural autoantibody positive (Q101018): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A ganglionopatia sensitiva autoimune ocorre como neuropatia sensitiva aguda, em associação com a síndrome de Sjögren também pansenssitiva, pequenas fibras , CANVAS (Ataxia cerebelar, neuropatia, síndrome de arreflexia vestibular), condições tóxicas como intoxicação por piridoxina e também tratamento com cisplatina devem ser considerados._x000D_ Tem um início subagudo, perda sensorial grave resultando em ataxia. O início pode ser assimétrico, geralmente começando nos braços e associado à dor neuropática. Uma vez estabelecido, tem curso crônico e ininterrupto, incapacitando o paciente. Anticorpo positivo: os perfis de anticorpos são atualmente desconhecidos.
@@ description / en / description / en @@
+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.
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+CID11:ID_1275925881
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+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-15T00:00:00Z
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@@ Property / Collection date: 15 August 2026 / rank @@
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Latest 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
default for all languages	ID_1275925881
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.