Rare Zebra

Rare disease search prototype built on Orphanet data

← Back to search

ORPHA:838

Susac syndrome

Also called Retinocochleocerebral vasculopathy

Body system
Neurological diseases
Inheritance pattern
Unknown
Typical age of onset
All ages
Estimated prevalence
Unknown (Worldwide)
Rarity class
Unknown

ORPHA:838 is classified under "Neurological diseases" in the Orphanet nomenclature.

Common signs

  • Headache
  • Sensorineural hearing impairment
  • Visual loss
  • Abnormal corpus callosum morphology
  • Confusion
  • Generalized hypotonia