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Спадковий fugax кератит

ORPHA:647815· ICD-10 H16.8· Keratitis fugax hereditaria

Визначення(English summary)

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.

Успадкування
Autosomal dominant