Long-term neurophysiological and clinical response in patients with chronic inflammatory demyelinating polyradiculoneuropathy treated with subcutaneous immunoglobulin

Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare immune-mediated disorder presenting with sub-acute onset and progressive symmetrical weakness over at least 2 months, involving proximal and distal limb muscles, associated with hypo/areflexia and impaired sensory functions (Latov, 2014; Koller et al., 2005).

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