Autoimmune autonomic ganglionopathy (AAG) is a rare form of dysautonomia in which the patient’s immune system produces ganglionic anti-nicotinic acetylcholine receptor (AChR) antibodies, inhibiting ganglionic AChR currents and impairing transmission in autonomic ganglia.[1] Symptoms onset can be acute, subacute or gradual.
https://en.wikipedia.org/wiki/Autoimmune_autonomic_ganglionopathy
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