An inherited condition affecting the cornea.
About Fuchs’ dystrophy
Fuchs dystrophy affects the cornea, which is the front part of the eye wall.
Fuchs’ dystrophy is an inherited problem with the pump layer of cells, which are responsible for pumping fluid back into the eye. The pump layer of cells line the inner aspect of the cornea and if they don’t function properly can cause the cornea to become waterlogged and cloudy.
Fuchs’ dystrophy is common and normally affects people in middle age or later life. The typical early symptom is ‘morning misting’ – patients find that their vision is misty on waking, but clears during the day.
Treatments for Fuchs’ dystrophy
Good vision can be restored in patients with Fuchs’ dystrophy and other causes of corneal endothelial failure by corneal transplantation.
Since 2000, selective corneal transplantation techniques have been developed which allow surgeons to replace the damaged endothelial layer with healthy tissue through a small, sutureless incision in an operation similar to modern cataract surgery.
Different versions of this operation called DSAEK or DMEK are available to suit different patients. These ‘keyhole’ corneal transplantation operations can be performed under local anaesthetic, can be repeated if necessary, and quickly improve vision.