epithelial-stromal TGFBI dystrophy lattice corneal dystrophy lattice corneal dystrophy type I corneal dystrophy, lattice type 3A https://rarediseases.info.nih.gov/diseases/10320/lattice-corneal-dystrophy-type-3a https://www.malacards.org/card/corneal_dystrophy_lattice_type_iiia lattice corneal dystrophy type 3A Lattice corneal dystrophy type 3A is rare condition that affects the cornea. It is characterized primarily by protein clumps in the clear, outer covering of the eye which cloud the cornea and impair vision. Affected people also experience recurrent corneal erosion (separation of certain layers of the cornea), which is associated with severe pain and sensitivity to bright light. Lattice corneal dystrophy type 3A is caused by changes (mutations) in the TGFBI gene and is inherited in an autosomal dominant manner. The condition is usually treated surgically. MESH:C563923 MEDGEN:332989 lattice corneal dystrophy type III A corneal dystrophy, lattice type IIIA OMIM:608471 MONDO:0012044 GARD:0010320 CDL3A UMLS:C1837974