corneal endothelial dystrophy type 2; congenital hereditary endothelial dystrophy of cornea; Maumemee corneal dystrophy

Pathology

• bilateral corneal dystrophy

Genetics

• autosomal recessive
• associated with defects in SLC4A11

Clinical manifestations

• corneal opacification
• nystagmus

More general terms

• corneal endothelial dystrophy; Chandler syndrome

Database

• OMIM: https://mirror.omim.org/entry/217700