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Neurology

Chronic inflammatory demyelinating polyradiculoneuropathy

Weakness worse proximally and distally over more than 8 weeks with demyelinating conduction studies. The EAN/PNS 2021 criteria, the mimics (anti-MAG, POEMS, MMN, CMT, amyloid), nodopathies, and IVIg, steroids and plasma exchange.

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At a glance

  • CIDP (chronic inflammatory demyelinating polyradiculoneuropathy, the EAN/PNS 2021 term; older texts say polyneuropathy) is a chronic immune-mediated demyelinating neuropathy of nerves and roots, progressing or relapsing over more than 8 weeks. Prevalence about 3 per 100,000, more in men and over 50.
  • Typical CIDP gives symmetric proximal and distal weakness with sensory loss and areflexia. Proximal weakness is the clue that it isn't a length-dependent neuropathy.
  • Diagnosis rests on demyelinating nerve conduction studies with clinical fit. It is over-diagnosed: in published referral series, around half of patients labelled CIDP didn't meet criteria.

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Last updated
14 November 2026
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