gelatinous drop-like corneal dystrophy; lattice corneal dystrophy type 3

Genetics

• autosomal recessive
• associated with defects in TACSTD2

Clinical manifestations

• grayish corneal amyloid deposits that cause severe visual impairment

More general terms

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

Database

• OMIM: https://mirror.omim.org/entry/204870