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Acute Immune Neuropathies: Facial Diplegia Variant (BFP)

Immune/Antibody
W
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antibody/gbs.htm#Acute Immune Neuropathies: Facial Diplegia Variant (BFP) 22

Overview

From WUSTL Neuromuscular

Epidemiology Japanese & North American patients Prodrome Infectious symptoms in previous 4 weeks Frequency: 86% URI or Fever most common Clinical Onset Age: 18 to 65 years Limb numbness Bifacial weakness Progressive: Over weeks Asymmetric: Often Paresthesias Most patients Distal limbs May persist for months Strength: Normal or Mildly reduced Tendon reflexes: Reduced or Absent Other cranial nerves: Often normal Course Monophasic Nadir at 4 weeks Improvement over months Differential diagnosis Laboratory CSF: Albumino-cytologic dissociation Protein: 51 to 256 Cells: 1 to 8 Nerve conduction studie

External Resources

WUSTL Neuromuscular
Washington University Disease Center
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.