Corneal dystrophies are currently classified according to the layer of corneal tissue that becomes abnormal.
Epithelial and sub-epithelial corneal dystrophies:
Epithelial basement membrane dystrophy
Also called map-dot-fingerprint dystrophy or Cogan’s dystrophy. This is the most common epithelial dystrophy and it causes pain, grittiness and blurred vision, which usually begins around the age of 30. Treatable with antibiotic drops and ointments and a bandage soft contact lens.
Meesmann’s corneal dystrophy
A very rare condition that does not often affect sight but that creates the feeling of grit in the eyes. It can be diagnosed in a baby under one but symptoms often do not start until the early 20s, or even middle age.
Bowman’s layer corneal dystrophies
Reis-Bucklers corneal dystrophy
Symptoms usually start in children who inherit it from one of their parents. Their vision becomes hazy because the corneal surface becomes very irregular. The eyes are sensitive to light and feel gritty; if damage to the corneal worsens, a corneal transplant may be recommended.
Thiel-Behnke corneal dystrophy
Symptoms begin in childhood or during the teen years. The epithelial surface of the cornea becomes irregular but sight loss is caused by white deposits in the Bowman’s layer.
Stromal corneal dystrophies
Granular dystrophy
Signs of dot-like deposits appear in the stroma of the cornea before the age of 20 but these do not start to affect vision for perhaps 30 years. Can be treated by a corneal transplant but the deposits can recur within 5 years.
Macular dystrophy
This can develop in the teens, with cloudy areas appearing in both corneas; a corneal transplant is often needed before the age of 30. The deposits can also recur but this takes much longer than in granular dystrophy; 20 years on average.
Lattice corneal dystrophy
Another corneal disease that occurs in relatively young people. Sight loss is less of a problem than the gritty feeling and pain that occurs in the eyes. A corneal graft is offered if vision loss is significant, but the donor cornea may become affected in 5-10 years. Other treatment aims to reduce the pain.
Descemet’s membrane and endothelial corneal dystrophies
Fuchs’ endothelial corneal dystrophy
This is the most common of the corneal dystrophies that affect the deeper layers of the cornea. Fuchs’ endothelial dystrophy tends to occur more often in women than in men but its genetics are complex. In someone who is affected, the endothelial cells deteriorate, causing the cornea to take on water.