Keratitis fugax hereditaria
ORPHA:647815· ICD-10 H16.8
Definition
A rare ophthalmic disorder characterized by periodic inflammatory attacks of the cornea manifesting as unilateral ocular pain, conjunctival hyperemia, photophobia and epiphora lasting for 1 to 3 days, followed by blurred vision for several weeks.
- Inheritance
- Autosomal dominant