congenital stromal corneal dystrophy (CSCD)

Pathology

• bilateral, primary alterations of the cornea
• not associated with prior inflammation or secondary to systemic disease

Genetics

• generally autosomal dominant
• associated with defects in decorin (DCN)

More general terms

• genetic disease of the eye
• corneal disease (keratopathy)

Database

• OMIM: https://mirror.omim.org/entry/610048