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