Isolated congenital sclerocornea
ORPHA:91490· ICD-10 Q13.3
Definition
A rare corneal disorder characterized by non-inflammatory, non-progressive, bilateral ingrowth of vascularized, opaque scleral tissue into the peripheral cornea, obliterating the corneoscleral limbus and scleral sulcus. The condition is not associated with other ocular abnormalities.
- Inheritance
- Autosomal dominant