Recurrent Miller Fisher syndrome: clinical and laboratory features and HLA antigens

K Chida1, H Nomura, H Konno

  • 1Department of Neurology, Kohnan Hospital, Sendai, Japan.

Insights

Recurrent Miller Fisher syndrome (MFS) shares clinical features with initial episodes and may be linked to HLA-DR2. Further research is needed to understand recurrence triggers in this rare neurological disorder.

Area of Science:

  • Neurology
  • Immunology

Background:

  • Miller Fisher syndrome (MFS) is a rare variant of Guillain-Barré syndrome.
  • Recurrence of MFS is uncommon, and its clinical characteristics and precipitating factors are not well understood.

Observation:

  • This study analyzed four cases of recurrent MFS among 28 Japanese MFS patients between 1981 and 1996.
  • Recurrent episodes occurred after long asymptomatic intervals (2.5–12.5 years) and presented with similar clinical and laboratory features to initial episodes.
  • Two recurrent patients tested positive for serum IgG anti-GQ1b antibody.

Findings:

  • All four recurrent MFS patients were positive for HLA-Cw3 and HLA-DR2.
  • The frequency of HLA-DR2 was significantly higher in recurrent MFS patients compared to healthy controls (corrected P = 0.038).
  • While HLA-DR2 was more frequent in recurrent MFS than non-recurrent cases, this difference was not statistically significant.

Implications:

  • Recurrent MFS appears clinically indistinguishable from typical MFS.
  • The human leukocyte antigen HLA-DR2 may be associated with an increased susceptibility to MFS recurrence.
  • Understanding genetic predispositions like HLA-DR2 could aid in predicting MFS recurrence risk.

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