# Miller Fisher Variant of Guillain-Barré Syndrome Presenting With Dysphagia and Ophthalmoplegia

**Authors:** Rupam Sharma, Sanjana Murdande, Jose Garcia-Corella, Arin Orogian, Linh Tran

PMC · DOI: 10.7759/cureus.100614 · Cureus · 2026-01-02

## TL;DR

This paper describes a rare case of Miller Fisher Syndrome, a variant of Guillain-Barré syndrome, where the patient initially showed dysphagia and ophthalmoplegia.

## Contribution

The paper highlights an unusual presentation of Miller Fisher Syndrome with dysphagia and ophthalmoplegia as initial symptoms.

## Key findings

- The patient presented with dysphagia and ophthalmoplegia as initial symptoms of Miller Fisher Syndrome.
- Dysphagia in combination with ophthalmoplegia is a rare presentation of Miller Fisher Syndrome.
- The case adds to the limited number of reported cases showing dysphagia as an initial symptom.

## Abstract

Miller Fisher syndrome (MFS) is a rare variant of Guillain-Barré syndrome (GBS). It is characterized by a triad of ataxia, areflexia, and ophthalmoparesis. Akin to GBS, it is often triggered by a respiratory infection, causing immune cross-activation against pathogenic proteins and gangliosides. Symptoms typically occur in chronological progression, beginning with ophthalmoparesis, then ataxia, and finally areflexia. Our case is of a patient presenting with dysphagia and ophthalmoplegia as the initial manifestations. There currently exist only a limited number of reported cases of MFS presenting with dysphagia, which, along with ophthalmoplegia, areflexia, and ataxia, should raise suspicion for MFS.

## Linked entities

- **Diseases:** Guillain-Barré syndrome (MONDO:0016218), Miller Fisher syndrome (MONDO:0005851)

## Full-text entities

- **Diseases:** areflexia (MESH:D000071699), respiratory infection (MESH:D012141), Dysphagia (MESH:D003680), MFS (MESH:D019846), ataxia (MESH:D001259), Ophthalmoplegia (MESH:D009886), GBS (MESH:D020275)
- **Chemicals:** gangliosides (MESH:D005732)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12758080/full.md

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Source: https://tomesphere.com/paper/PMC12758080