Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:98919

Miller Fisher syndrome

Also called Cranial variant of GBS, Cranial variant of Guillain-Barré syndrome, Fisher syndrome

Body system
Neurological diseases
Inheritance pattern
Multigenic/multifactorial, Not applicable
Typical age of onset
All ages
Estimated prevalence
1-9 / 1 000 000 (Europe)
Rarity class
1-9 / 1 000 000

ORPHA:98919 is classified under "Neurological diseases" in the Orphanet nomenclature.

Common signs

  • External ophthalmoplegia
  • Areflexia
  • Anti-GQ1b antibody positivity
  • Diplopia
  • Horizontal nystagmus
  • Ataxia