Autoimmune autonomic ganglionopathy

A rare variant of Guillain-Barré syndrome characterized by acute post-ganglionic sympathetic and parasympathetic failure presenting several weeks after acute infection with gastrointestinal symptoms (abdominal pain, vomiting, constipation, diarrhea, gastroparesis, ileus), orthostatic hypotension, erectile dysfunction, urinary frequency, urgency or retention, vasomotor instability with acrocyanosis and reduced salivation, lacrimation and sweating.

Also known as: AAG, acute panautonomic GBS, acute panautonomic Guillain-Barre syndrome, acute panautonomic Guillain-Barré syndrome, acute panautonomic neuropathy, acute pandysautonomia, autoimmune autonomic neuropathy, idiopathic subacute autonomic neuropathy

39 clinical trials for this condition and its sub-types, 1 tagged with Autoimmune autonomic ganglionopathy itself.