Fuchs'
dystrophy
Overview
In Fuchs' (fewks) dystrophy, fluid builds up
in the clear layer (cornea) on the front of your eye, causing your cornea to
swell and thicken. This can lead to glare, blurred or cloudy vision, and eye
discomfort.
Fuchs' dystrophy usually affects both eyes and
can cause your vision to gradually worsen over years. Typically, the disease
starts in the 30s and 40s, but many people with Fuchs' dystrophy don't develop
symptoms until they reach their 50s or 60s.
Some medications and self-care steps may help
relieve your Fuchs' dystrophy signs and symptoms. But when the disorder is
advanced and your vision is affecting your ability to function well, the best
way to restore vision is with cornea transplant surgery.
Symptoms
As the disease progresses, Fuchs' dystrophy
symptoms, which usually affect both eyes, might include:
·
Blurred or cloudy
vision, sometimes described as a general lack of clarity of vision.
·
Fluctuation in vision,
with worse symptoms in the morning after awakening and gradually improving
during the day. As the disease progresses, blurred vision either can take
longer to improve or doesn't improve.
·
Glare, which can
decrease your vision in dim and bright light.
·
Seeing halos around
lights.
·
Pain or grittiness
from tiny blisters on the surface of your cornea.
When to see a doctor
If you have some of these symptoms, and
especially if they worsen over time, see an eye care provider, who might then
refer you to a corneal specialist. If symptoms develop suddenly, call for an urgent
appointment. Other eye conditions that cause the same symptoms as Fuchs'
dystrophy also require prompt treatment.
Causes
Normally, the cells lining the inside of the
cornea (endothelial cells) help maintain a healthy balance of fluid within the
cornea and prevent the cornea from swelling. But with Fuchs' dystrophy, the
endothelial cells gradually die or do not work well, resulting in fluid buildup
(edema) within the cornea. This causes corneal thickening and blurred vision.
Fuchs' dystrophy is usually inherited. The
genetic basis of the disease is complex — family members can be affected to
varying degrees or not at all.
Risk factors
Factors that increase your risk of developing
Fuchs' dystrophy include:
·
Sex. Fuchs' dystrophy is more common in women
than in men.
·
Genetics. Having a family history of Fuchs'
dystrophy increases your risk.
·
Age. Although there's a rare early-onset type
of Fuchs' dystrophy that begins in childhood, typically the disease starts in
the 30s and 40s, with symptoms developing thereafter.
Diagnosis
Besides testing your vision, your doctor might
also have you undergo the following tests to determine whether you have Fuchs'
dystrophy:
·
Cornea
examination and grading. Your
doctor will make the diagnosis of Fuchs' dystrophy by examining your eye with
an optical microscope (slit lamp) to look for irregular bumps (guttae) on the
inside surface of the cornea. He or she will then assess your cornea for
swelling and stage your condition.
·
Corneal
thickness. Your doctor
might use a test called corneal pachymetry to measure the thickness of the
cornea.
·
Corneal
tomography. Your doctor
might obtain a special photograph of your cornea (tomography) to assess for
early signs of swelling in your cornea.
·
Corneal
cell count. Sometimes your
doctor might use a special instrument to record the number, shape and size of
the cells that line the back of the cornea. However, this test is not required.
Treatment
Some nonsurgical treatments and self-care
strategies might help relieve the symptoms of Fuchs' dystrophy. If you have
severe disease, your doctor might suggest surgery.
Medications and other
therapies
·
Eye
medication. Saline (5%
sodium chloride) eyedrops or ointments can help reduce the amount of fluid in
your cornea.
·
Soft
contact lenses. These act as a
covering to relieve pain.
Surgery
People who have surgery for advanced Fuchs'
dystrophy can have much better vision and remain symptom-free for years
afterward. Surgical options include:
·
Transplanting
the inner layer of the cornea. Known as Descemet membrane endothelial keratoplasty
(DMEK), this procedure involves replacing the back layer of the cornea with
healthy endothelial cells from a donor. The procedure is usually done with
local anesthesia in an outpatient setting.
·
Transplanting
the cornea. If you have
another eye condition or have had previous eye surgery, DMEK may not
be an option. Your doctor may recommend a partial-thickness cornea transplant,
a procedure known as Descemet-stripping endothelial keratoplasty (DSEK). Rarely,
a full-thickness cornea transplant, known as penetrating keratoplasty (PK), may
be recommended.
Potential future
treatments
A variety of new treatments are being
investigated that could change how Fuchs' dystrophy is managed in the future.
After the genetic abnormality associated with most cases of Fuchs' dystrophy
was discovered, there is a better understanding of how the disease might
develop, and this offers the potential for nonsurgical therapies in the future.
Various eyedrop treatments are being developed and may enter clinical trials in
the future. Novel surgical treatments also are being studied to determine if
they may be of benefit.
Lifestyle and home
remedies
In addition to following your doctor's
instructions for care, you can try these techniques to help reduce glare or
soothe your eyes.
·
Apply over-the-counter
(nonprescription) salt solution (5% sodium chloride) eyedrops or ointment.
·
Dry your eyes with a
hair dryer. Hold it at arm's length and direct warm — not hot — air across your
face, especially in the morning when swelling is worse. This helps remove
excess fluid in the cornea, which decreases swelling.
Preparing for your
appointment
If you suspect that you have Fuchs' dystrophy,
make an appointment to see an eye care provider (optometrist or ophthalmologist).
In some cases, you might be referred to an ophthalmologist who specializes in
corneal disease.
Here's information to help you get ready for
your appointment.
What you can do
Make a list of:
·
Your
symptoms, and when they
began
·
Key
personal information, including family
history of eye conditions
·
All
medications, vitamins or
other supplements you take and dose
·
Questions
to ask your doctor
Take a family member or a friend along, if
possible. You might not want to drive yourself home if your pupils have been
dilated for the exam, and your companion can help you remember information you
get during your appointment.
For Fuchs' dystrophy, questions to ask your
doctor include:
·
What else could cause
my symptoms?
·
How will my vision be
affected?
·
How rapidly will my condition
progress?
·
What tests do I need?
·
What treatments are
available, and what do you recommend?
·
I have these other
health conditions. How can I manage them together?
·
Do I need to restrict
my activities?
·
Are there brochures or
other printed material I can have? What websites do you recommend?
Don't hesitate to ask other questions.
What to expect from
your doctor
Your doctor is likely to ask you questions,
such as:
·
Have your symptoms
been continuous or occasional?
·
How severe are your
symptoms?
·
What, if anything,
seems to improve your symptoms?
·
What, if anything,
appears to worsen your symptoms?
·
Do your symptoms
change throughout the day?
·
Have you noticed
changes in your vision?
·
Does your vision seem
worse in the morning and improve during the day?
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