Miller Fisher syndrome

disease
On this page

Also known as cranial variant of GBScranial variant of Guillain-Barre syndromecranial variant of Guillain-Barré syndromeFisher syndromeGuillain Barre syndrome, Miller Fisher variantGuillain-Barre syndrome, Miller Fisher variantMiller Fisher variant of Guillain Barre syndromeMiller-Fisher syndromeophthalmoplegia, ataxia and areflexia syndromesyndrome, Fishersyndrome, Miller Fishersyndrome, Miller-Fisher

Summary

Miller Fisher syndrome (MONDO:0005851) is a disease and 2 clinical trials. Top therapeutic interventions include fibrinogen, human. A subtype of autoimmune disorder of central nervous system — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: 1-9 / 1 000 000 (Europe) [Orphanet-validated]
  • Phenotypes (HPO): 26
  • Clinical trials: 2

Clinical features

Epidemiology

Prevalence records

2 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Annual incidence1-9 / 1 000 0000.1EuropeValidated
Point prevalence1-9 / 1 000 000EuropeNot yet validated

Signs & symptoms

Clinical features (HPO)

26 HPO clinical features (Orphanet curated; top 26 by frequency):

HPO IDTermFrequency
HP:0000544External ophthalmoplegiaVery frequent (80-99%)
HP:0001284AreflexiaVery frequent (80-99%)
HP:0034122Anti-GQ1b antibody positivityVery frequent (80-99%)
HP:0000651DiplopiaFrequent (30-79%)
HP:0000666Horizontal nystagmusFrequent (30-79%)
HP:0001251AtaxiaFrequent (30-79%)
HP:0002922Increased CSF protein concentrationFrequent (30-79%)
HP:0003457EMG abnormalityFrequent (30-79%)
HP:0007942Internal ophthalmoplegiaFrequent (30-79%)
HP:0010845EEG with generalized slow activityFrequent (30-79%)
HP:0011499MydriasisFrequent (30-79%)
HP:0000613PhotophobiaOccasional (5-29%)
HP:0000622Blurred visionOccasional (5-29%)
HP:0001283Bulbar palsyOccasional (5-29%)
HP:0001945FeverOccasional (5-29%)
HP:0002273TetraparesisOccasional (5-29%)
HP:0002315HeadacheOccasional (5-29%)
HP:0003401ParesthesiaOccasional (5-29%)
HP:0004372Reduced consciousness/confusionOccasional (5-29%)
HP:0009916AnisocoriaOccasional (5-29%)
HP:0010628Facial palsyOccasional (5-29%)
HP:0011347Abnormality of ocular abductionOccasional (5-29%)
HP:0012229CSF pleocytosisOccasional (5-29%)
HP:0000508PtosisVery rare (<1-4%)
HP:0002013VomitingVery rare (<1-4%)
HP:0002015DysphagiaVery rare (<1-4%)

Identifiers

Disease identifiers

FieldValue
Canonical nameMiller Fisher syndrome
Mondo IDMONDO:0005851
EFOEFO:0007371
MeSHD019846
Orphanet98919
DOIDDOID:12889
ICD-11134795253
NCITC116958
SNOMED CT1767005
UMLSC0393799
MedGen95994
GARD0003668
MedDRA10049567
Is cancer (heuristic)no

Also known as: cranial variant of GBS · cranial variant of Guillain-Barre syndrome · cranial variant of Guillain-Barré syndrome · Fisher syndrome · Guillain Barre syndrome, Miller Fisher variant · Guillain-Barre syndrome, Miller Fisher variant · Miller Fisher variant of Guillain Barre syndrome · Miller-Fisher syndrome · ophthalmoplegia, ataxia and areflexia syndrome · syndrome, Fisher · syndrome, Miller Fisher · syndrome, Miller-Fisher

Disease family

This is a subtype of autoimmune disorder of central nervous system. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › nervous system disordercentral nervous system disorderautoimmune disorder of central nervous systemMiller Fisher syndrome

Related subtypes (7): multiple sclerosis, autoimmune encephalopathy with parasomnia and obstructive sleep apnea, lymphocytic hypophysitis, autoimmune encephalitis, autoimmune optic neuritis, central nervous system lupus, autoimmune epilepsy

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 2.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified2

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01582763Not specifiedCOMPLETEDInternational Guillain-Barré Syndrome Outcome Study
NCT03801135Not specifiedUNKNOWNChanges in Haemostasis After Therapeutic Plasmapheresis With Citrate Anticoagulation

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
FIBRINOGEN, HUMAN31