Abstract
Autoimmune autonomic ganglionopathy (AAG) is a rare disease mediated by antibodies causing severe orthostatic-hypotension. Due to its unique presentation, patients can go undiagnosed causing them profound disability and poor-quality of life. Our case of AAG presenting in a 69-year-old-female illustrates the importance of including AAG in the differential diagnosis for patients who present with autonomic dysfunction.
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