posterior polymorphous corneal dystrophy 1

info · Genetic · ICD-10: H18.50

A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.

Signs and symptoms

Epiphora
Corneal opacity
Band keratopathy
Polymorphous posterior corneal dystrophy
Abnormal corneal endothelium morphology
Abnormal Descemet membrane morphology
Anterior synechiae of the anterior chamber
Photophobia
Uveal ectropion
Glaucoma

Also known as: CHED1; Corneal Endothelial Dystrophy 1, Autosomal Dominant; Maumenee Corneal Dystrophy; PPCD1