Polyneuropathy associated with anti-MAG IgM antibodies
Patients with anti-MAG neuropathy typically have an insidiously progressive, distal and symmetrical, sensory or sensorimotor neuropathy. The disorder usually afflicts men over the age of 60 years. Initial features include acral numbness, paresthesias, reduced proprioception, and Romberg sign. Sensory ataxia occurs in half of the cases and often is the most disabling symptom.
Jan. 05, 2021