Autoimmune sensory neuropathy (Q85110): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A neuropatia autonômica e sensitiva aguda é caracterizada por comprometimento autonômico e sensitiva sem disfunção motora que atinge seu nadir em um curto período de tempo. O curso clínico monofásico e a presença frequente de história de infecções antecedentes sugerem um mecanismo imunológico. Os sintomas iniciais são aqueles relacionados a distúrbios autonômicos ou comprometimento sensitivo superficial, enquanto o comprometimento sensitivo profundo acompanhado de ataxia sensitiva aparece posteriormente. Casos de autópsia mostram perda neuronal nos gânglios simpáticos torácicos e da raiz dorsal. Pequenos neurônios nos gânglios autonômicos e sensitivos podem ser afetados na fase inicial e, subsequentemente, grandes neurônios nos gânglios sensitivos são danificados na neuropatia autonômica e sensitiva aguda.
@@ description / en / description / en @@
+Acute autonomic and sensory neuropathy is characterised by autonomic and sensory impairment without motor dysfunction that reaches its nadir within a short period of time. The monophasic clinical course and frequent presence of a history of antecedent infections suggests an immune mechanism. The initial symptoms are those related to autonomic disturbance or superficial sensory impairment, while deep sensory impairment accompanied by sensory ataxia subsequently appears later. Autopsy cases show neuronal loss in the thoracic sympathetic and dorsal root ganglia. Small neurons in the autonomic and sensory ganglia may be affected in the initial phase and, subsequently, large neurons in the sensory ganglia are damaged in acute autonomic and sensory neuropathy.
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
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@@ Property / Collection date: 13 August 2026 / rank @@
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Latest revision as of 10:28, 15 August 2026

Acute autonomic and sensory neuropathy is characterised by autonomic and sensory impairment without motor dysfunction that reaches its nadir within a short period of time. The monophasic clinical course and frequent presence of a history of antecedent infections suggests an immune mechanism. The initial symptoms are those related to autonomic disturbance or superficial sensory impairment, while deep sensory impairment accompanied by sensory ataxia subsequently appears later. Autopsy cases show neuronal loss in the thoracic sympathetic and dorsal root ganglia. Small neurons in the autonomic and sensory ganglia may be affected in the initial phase and, subsequently, large neurons in the sensory ganglia are damaged in acute autonomic and sensory neuropathy.

Language	Label	Description	Also known as
default for all languages	ID_123162186
English	Autoimmune sensory neuropathy	Acute autonomic and sensory neuropathy is characterised by autonomic and sensory impairment without motor dysfunction that reaches its nadir within a short period of time. The monophasic clinical course and frequent presence of a history of antecedent infections suggests an immune mechanism. The initial symptoms are those related to autonomic disturbance or superficial sensory impairment, while deep sensory impairment accompanied by sensory ataxia subsequently appears later. Autopsy cases show neuronal loss in the thoracic sympathetic and dorsal root ganglia. Small neurons in the autonomic and sensory ganglia may be affected in the initial phase and, subsequently, large neurons in the sensory ganglia are damaged in acute autonomic and sensory neuropathy.