Korean J Ophthalmol.  2016 Aug;30(4):314-315. 10.3341/kjo.2016.30.4.314.

Recurrent Ophthalmoplegia Presenting Different Clinical Features in a Patient with Anti-GQ1b Antibody Syndrome

Affiliations
  • 1Department of Ophthalmology, Gil Medical Center, Gachon University, Incheon, Korea.
  • 2Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. htlim@amc.seoul.kr

Abstract

No abstract available.


MeSH Terms

Adult
Autoantibodies/*blood
Gangliosides/blood/*immunology
Humans
Male
Ophthalmoplegia/blood/*diagnosis/immunology
Recurrence
Syndrome
Autoantibodies
Gangliosides

Figure

  • Fig. 1 Five days after the onset of diplopia, a -1 limitation of abduction and a -1 limitation of adduction with gaze-evoked nystagmus were noted in both eyes. Vertical gaze was intact.


Reference

1. Odaka M, Yuki N, Hirata K. Anti-GQ1b IgG antibody syndrome: clinical and immunological range. J Neurol Neurosurg Psychiatry. 2001; 70:50–55.
2. Odaka M, Yuki N, Yamada M, et al. Bickerstaff's brainstem encephalitis: clinical features of 62 cases and a subgroup associated with Guillain-Barre syndrome. Brain. 2003; 126(Pt 10):2279–2290.
3. Fisher M. An unusual variant of acute idiopathic polyneuritis (syndrome of ophthalmoplegia, ataxia and areflexia). N Engl J Med. 1956; 255:57–65.
4. Hamaguchi T, Yamaguchi K, Komai K, et al. Recurrent anti-GQ1b IgG antibody syndrome showing different phenotypes in different periods. J Neurol Neurosurg Psychiatry. 2003; 74:1350.
5. Ito M, Kuwabara S, Odaka M, et al. Bickerstaff's brainstem encephalitis and Fisher syndrome form a continuous spectrum: clinical analysis of 581 cases. J Neurol. 2008; 255:674–682.
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