Fuchs’ dystrophy affects the cornea, over time causing decline in vision due to corneal edema and clouding. Fuchs’ dystrophy is an eye disease that occurs when the innermost layers of corneal cells begin to change. This layer of cells is responsible for the maintenance of proper fluid in the cornea. Known as the endothelium, it keeps the cornea clear in order to provide clear vision and removes excess fluid that could cause corneal swelling.
As Fuchs’ dystrophy progresses, it can lead to blisters on the cornea and swelling.
Unfortunately, Fuchs’ dystrophy is unpreventable, but there are treatments available to help slow down disease progression and maintain proper vision.
Fuchs’ dystrophy has genetic causes, as it has been found to run in families. On the other hand, there have been cases of Fuchs’ dystrophy without any family history of the condition. In many cases, the cause of Fuchs’ dystrophy is unknown.
In Fuchs’ dystrophy, the endothelium cells begin to die off and do not function properly, causing the fluid to build up and the cornea to become thicker, which contributes to the symptoms related to the eye disease.
Risk factors include being a female, having a family history of the condition, and being over the age of 50.
Complications arising from Fuchs’ dystrophy include glaucoma, expulsive hemorrhage, cataracts, graft rejection and failure, wound separation, aqueous leaks, loose sutures, infected keratitis, endophthalmitis, epithelial healing problems and ulceration, and retinal detachment.
Fuchs’ dystrophy commonly affects both eyes, so the symptoms a patient may experience include:
You should see a doctor right away if you begin to experience any of these symptoms, especially if they begin to worsen. The sooner the treatment starts, the better the outcome for Fuchs’ dystrophy will be.
There are three main stages of Fuchs’ dystrophy.
Stage 1 (Cornea guttata): Symptoms are mild or non-existent, pigment dusting is noticeable. Vision may be worse in the morning, but generally patients don’t experience any problems in this stage.
Stage 2: There is an increase in visual problems experienced, and patients may see halos or blurred vision and glares. There is a greater risk of infectious keratitis in stage two, and patients may experience the sensation of having a foreign body in the eye.
Stage 3: Corneal transplant may be necessary as symptoms are much worse and vision is limited.
Treatment of Fuchs’ dystrophy depends on its stage. In the early stage, vision can be improved by removing excess fluid with the assistance of eye drops. If Fuchs’ dystrophy occurs along with ocular hypertension, your doctor may also recommend glaucoma eye drops to help relieve pressure, as high eye pressure can damage the corneal endothelium.
If the disease has progressed, and there is vision deterioration and pain, a corneal transplant may be required. Normally, the surgery replaces the entire cornea, but there is an alternative surgery that only replaces the endothelium without touching the cornea. This has shown to be successful in treating Fuchs’ dystrophy with fewer risks, too.
In order to successfully diagnose Fuchs’ dystrophy, your doctor will perform a visual test, determine the stage of your condition using an optical microscope, perform a corneal pressure test by numbing the eye and measuring pressure with a device, use an instrument to measure corneal thickness, and perform a corneal cell count, which is also conducted using a special instrument.
As mentioned, there are no known prevention tips for Fuchs’ dystrophy, but there are some precautions to keep in mind.
Also speak to your doctor if you were planning on undergoing laser eye surgery or if you have to undergo cataract surgery. These types of eye procedures can worsen Fuchs’ dystrophy, so you may not be able to undergo such surgeries.