This document summarizes myelin-associated glycoprotein (MAG) neuropathy. It presents as a chronic, slowly progressive large-fiber sensory-motor polyneuropathy, usually affecting the lower extremities initially. Diagnosis involves detecting anti-MAG antibodies and demonstrating demyelination on electrophysiology. While the condition progresses slowly over decades, it can ultimately cause significant muscle weakness, wasting, and ataxia. Current treatments focus on B cell depleting therapies like rituximab, while future therapies may involve antigen-specific immunotherapy.