Lattice corneal dystrophy
（重定向自Finnish type amyloidosis）
![](/Images/godic/202501/13/Lattice_corneal_dystrophy_type_12811.JPEG")
![Lattice corneal dystrophy type II. Black and white light micrograph showing deposits of amyloid in cornea. Congo red stain.](/Images/godic/202501/13/Lattice_corneal_dystrophy_type_II_cornea_cut2811.jpg")
![Diagram depicting gelsolin and the amyloid protein derived from it because of mutations in codon](/Images/godic/202501/13/Lattice_corneal_dystrophy_type_II_diagram2811.gif")
Lattice corneal dystrophy type, also known as Biber-Haab-Dimmer dystrophy, is a rare form of corneal dystrophy. It has no systemic manifestations, unlike the other type of the dystrophy, Lattice corneal dystrophy type II. Lattice corneal dystrophy was first described by Swiss ophthalmologist Hugo Biber in 1890.