Related Experiment Video
Updated: Aug 15, 2026

Multifocal Electroretinograms
Published on: December 4, 2011
[Recurrent Miller-Fisher syndrome]
F Battaglia1, F Attane, A Robinson
1Service de Neurologie, Centre Hospitalier A. Gayraud, Carcassonne. fabrice.battaglia@ch-carcassonne.fr
Introduction:
Miller-Fisher syndrome (MFS) is a rare auto-immune post-infectious syndrome, characterized by an ataxia, an ophthalmoplegia and a generalized areflexia. It is considered as a clinical variant of Guillain-Barré syndrome (GBS). MFS is correlated with the presence of anti-GQ1b antibodies, elevated cerebrospinal fluid (CSF) protein levels, presence of mostly sensitive electrophysiological abnormalities and for some authors central involvement with increased signal intensity of brainstem and cerebellum on MRI. Recurrent MFS is extremely rare with only 21 cases since the first description in 1970.
Case Report:
A 54-year-old women presented MFS with two episodes in 19 years. Clinically, the first episode was a "classical" MFS, and the second an extensive MFS with tetraparesis and respiratory failure. CSF protein levels and cerebral MRI were normal. Anti-GQ1b antibodies were strongly positive and anti-GM1, anti-GM2 antibodies were slightly positive, campylobacter jejuni serology was negative. Electromyography showed isolated sensory abnormalities in median nerves territory.
Conclusion:
We report a new case of recurrent MFS with unusual clinical, biological and electrophysiological features.
Insights
Recurrent Miller-Fisher syndrome (MFS) is exceptionally rare. This case highlights unusual clinical, biological, and electrophysiological features in a patient with two MFS episodes over 19 years.
Area of Science:
- Neurology
- Autoimmune Disorders
Background:
- Miller-Fisher syndrome (MFS) is a rare autoimmune post-infectious neurological disorder.
- It is characterized by ataxia, ophthalmoplegia, and areflexia, often considered a variant of Guillain-Barré syndrome (GBS).
- MFS is typically associated with anti-GQ1b antibodies and electrophysiological abnormalities.
Observation:
- A 54-year-old woman experienced two episodes of MFS over 19 years.
- The first episode presented as classical MFS, while the second was extensive, involving tetraparesis and respiratory failure.
- This patient had normal CSF protein levels and brain MRI findings.
Findings:
- The patient exhibited strongly positive anti-GQ1b antibodies and slightly positive anti-GM1/anti-GM2 antibodies.
- Electromyography revealed isolated sensory abnormalities in the median nerve territory.
- Campylobacter jejuni serology was negative, ruling out a common trigger.
Implications:
- This case expands the understanding of recurrent MFS, demonstrating unusual clinical presentations.
- It underscores the importance of considering atypical features in recurrent MFS diagnosis.
- The findings contribute to the literature on the variable clinical and biological spectrum of MFS.
Related Concept Videos
Rocky Mountain Spotted Fever
Viral Meningitis
Cardiomyopathy IV: Restrictive Cardiomyopathy
Multiple Sclerosis l: Introduction
Epilepsy ll: Types
Sex Linked Disorders
