Prevalence and Patterns of Cranial Nerve Involvement in CIDP, Autoimmune Nodopathy, MMN, and Anti-MAG Neuropathy: A Multicenter Korea/UK study of 582 patients

  • Young Gi Min
  • , Hyunjin Kim
  • , Hee Jo Han
  • , Byeol-A. Yoon
  • , Jong Kuk Kim
  • , Woohee Ju
  • , Seok-Jin Choi
  • , Sung-Min Kim
  • , Ki Hoon Kim
  • , Young Nam Kwon
  • , Seung Woo Kim
  • , Eun-Jae Lee
  • , Young-Min Lim
  • , Kabir K. Nazeer
  • , Yusuf A. Rajabally*
  • , Ha Young Shin
  • , Jung-Joon Sung
  • *Corresponding author for this work

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Abstract

Background
Cranial nerve involvement is a well-recognized feature in Guillain–Barré syndrome (GBS) but remains less well understood in chronic forms of autoimmune neuropathies. Earlier studies of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) were conducted before updated diagnostic criteria and the recognition of autoimmune nodopathy (AN), which may limit the interpretation of their findings.

Methods
We retrospectively analyzed 582 patients with chronic autoimmune neuropathies—CIDP (n = 431), multifocal motor neuropathy (MMN) (n = 64), anti-myelin-associated glycoprotein (MAG) neuropathy (n = 54), and AN (n = 33)—from 4 Korean and 1 UK centers. Patients with cranial nerve involvement were identified and described. CIDP patients with cranial nerve involvement (cranial+ CIDP) were compared with those without (cranial− CIDP).

Results
Cranial nerve involvement was observed in 8.8% (38/431) of CIDP and 24.2% (8/33) of AN patients but was absent in MMN (0/64) and anti-MAG neuropathy (0/54). Facial palsy was overall the most common manifestation (CIDP: 45%, AN: 50%). Patients with AN more frequently exhibited bilateral optic neuropathy (50%) and facial diplegia (38%), while CIDP patients more often showed trigeminal neuropathy and oculomotor nerve palsy (both 32%). Compared with cranial− CIDP, cranial+ CIDP patients were more often younger, of variant subtypes (especially multifocal), presented (sub)acutely with preceding infection/vaccination, followed by relapsing–remitting rather than progressive courses, and achieved greater improvement despite greater pre-treatment disability.

Conclusions
Cranial nerve involvement serves as a diagnostic clue in chronic autoimmune neuropathies, particularly in identifying AN and CIDP. Cranial+ CIDP appears to represent a distinct subset with partial overlap to GBS, suggesting unique underlying mechanisms.
Original languageEnglish
Article numbere70512
Number of pages8
JournalEuropean Journal of Neurology
Volume33
Issue number2
Early online date9 Feb 2026
DOIs
Publication statusPublished - 9 Feb 2026

Bibliographical note

Copyright © 2026 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Funding

This work was supported by the National Research Foundation of Korea grant funded by the South Korea government (RS-2023-00212125, RS-2025-00553428, RS-2025-25467802), and Asan Institute for Life Science, Asan Medical Center, Seoul, South Korea (2024IP0071).

FundersFunder number
Seoul National University Hospital
National Research Foundation of KoreaRS-2023-00212125, RS-2025-25467802, RS-2025-00553428
2024IP0071

    Keywords

    • AN
    • CIDP
    • MMN
    • anti-MAG neuropathy
    • cranial nerve

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