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Activity of Posterior Lateral Line Afferent Neurons during Swimming in Zebrafish
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The pescatorial sixth.

Francesco Pellegrini1, Giovanni Prosdocimo2, Jason J S Barton3

  • 1Neuro-Ophthalmology Service, Department of Ophthalmology, Conegliano Hospital, Conegliano, Treviso, Italy.

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Summary
This summary is machine-generated.

Miller-Fisher syndrome, a rare autoimmune disorder, can present with ophthalmoplegia (paralysis of eye muscles) and ataxia (loss of coordination). This case highlights a variant without ataxia, emphasizing the need for prompt diagnosis in patients with bilateral VI nerve palsies.

Keywords:
Miller-Fisher syndromeareflexiadiplopiaophthalmoplegiasixth nerve palsy

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Area of Science:

  • Neurology
  • Autoimmune Diseases
  • Ophthalmology

Background:

  • Miller-Fisher syndrome (MFS) is a rare variant of Guillain-Barré syndrome, characterized by ophthalmoplegia, ataxia, and areflexia.
  • The classic MFS triad is often preceded by infectious triggers, such as gastroenteritis.

Observation:

  • A 56-year-old male with diabetes presented with acute diplopia and bilateral complete abduction deficits.
  • Initial examination revealed diffuse areflexia; however, the patient subsequently developed complete ophthalmoplegia and ataxia.
  • A history of possible gastroenteritis 3 weeks prior to symptom onset was elicited.

Findings:

  • The clinical presentation was consistent with Miller-Fisher syndrome.
  • This case illustrates an atypical "ophthalmoplegia without ataxia" variant of MFS.
  • Bilateral VI nerve palsies were a key presenting feature.

Implications:

  • The "ophthalmoplegia without ataxia" variant of MFS should be considered in the differential diagnosis of patients presenting with bilateral VI nerve palsies.
  • Early recognition and diagnosis of MFS variants are crucial for timely management and improved patient outcomes.
  • Understanding atypical presentations of MFS aids in refining diagnostic criteria and treatment strategies for autoimmune neuropathies.