Fuchs’ Dystrophy

Fuchs’ Dystrophy is a rare corneal disease that causes excess fluid buildup in the cornea. It is a slowly-progressing disease, the cause of which is unknown. The disease is usually passed on from a parent who suffers from the condition.

The cornea is made up of several layers, including the most inner layer, the endothelium. In a healthy cornea, the endothelial cells act as a pump or filter, draining any excess fluid from the cornea in order to maintain its clarity.

Fuchs’ Dystrophy affects these endothelial cells, causing them to deteriorate and eventually die. The result is a less effective drainage pump and fluid buildup in the cornea. This fluid buildup causes a number of reactions, including swelling, pain, cloudiness and eventually reduced vision.

Am I at Risk?

The actual cause of Fuchs’ Dystrophy is unknown, but it is apparent that the disease is hereditary. However, the degree of which one family member experiences symptoms can vary greatly, so it is not uncommon for a person to pass along the disease unknowingly to their offspring.

People more likely to develop the disease include:

  • Women – who are 5 times more likely to develop the disease then men
  • People with an immediate family member who has the disease
  • People over the age of 50

Symptoms

The symptoms of Fuchs’ Dystrophy usually don’t appear in people until they are age 50 or older, although in some cases they can appear sooner. They include:

  • Blurry or distorted vision
  • Impaired night vision
  • Light sensitivity
  • The appearances of glare and halos around lights
  • Pain/pressure in your eyes
  • Tiny blisters on your eyes
  • Your eyes look cloudy in the mirror
  • Vision that is cloudy in the morning and clears up as you go through the day
  • View Video

Treatment

Luckily, Fuch’s Dystrophy can often be treated with Descemet’s Membrane Endothelial Keratoplasty (DMEK) surgery. DMEK is the most exciting option available to treat the decreased vision and swollen, cloudy corneas seen in Fuchs’ Dystrophy. DMEK has been shown to offer patients the best chance to see 20/25 or better, resume normal activities quickly, and avoid vision-threatening rejection episodes. This is because DMEK is the most anatomical repair possible – just one cell layer (the endothelial cells) and a thin membrane all of which is only 15 to 20 microns thick.

Price Vision Group patient Ninja Von Oertzen provided us with these “Before and after” images illustrating her experience with Fuch’s Dystrophy and her improvement after treatment with DMEK surgery at Price Vision Group:

NvO_DMEK_textures_1fuchsNvO_DMEK_textures_2020

NvO_DMEK_remotes_1fuchs NvO_DMEK_remotes_2020

NvO_DMEK_potholes_1fuchs NvO_DMEK_potholes_2020

NvO_DMEK_NYC_1fuchsNvO_DMEK_NYC_2020

NvO_DMEK_nutrition_1fuchs NvO_DMEK_nutrition_2020

NvO_DMEK_brooklyn_1fuchs NvO_DMEK_brooklyn_2020

These symptoms usually affect both eyes, and gradually worsen over time. Additionally, these symptoms are concerns for a variety of eye problems, so if you are experiencing any of these, it is advised that you schedule an appointment with your eye doctor immediately.

Feel free to call us at (800) 317-3937 or e-mail us with your questions, concerns, and to schedule an appointment if you’re ready.

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Indianapolis, IN
(800) 317-3937

Price Vision Group 9002 North Meridian Street #100
Indianapolis, IN 46260
Monday–Friday: 8 a.m.–5 p.m.
(317) 844-5530


Price Vision Group is a global leader in corneal transplant, cataract surgery, keratoconus treatment, PRK and LASIK. At our center in Indianapolis, we see patients from Indiana cities including Fishers, Carmel, Noblesville, Avon, and Greenwood, as well as people who travel from across the U.S. and even abroad for treatment by our renowned physicians.

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