There is evidence to suggest that keratoconus has a genetic component. If you have a family history of the condition, your risk increases. However, the genetic mechanisms are complex and not fully understood.
Given the recent findings from the Gutenberg Health Study, with a prevalence of keratoconus now estimated to be 1 in 200 among Caucasians, it's now likely that over 650,000 Americans, within just the Caucasian population in the United States, could be affected by keratoconus.
Keratoconus is a progressive eye disease that affects the cornea, which is the front part of your eye. Over time, the cornea becomes thinner and begins to bulge outward into a cone-like shape. This change results in an irregular corneal surface and causes a variety of symptoms such as blurred vision, distortions, and eye redness.
Keratoconus can lead to a host of symptoms, which may include:
The exact cause of keratoconus isn't entirely known. However, it's believed to be a complex condition that may have a genetic component. A family history of keratoconus could increase your risk of developing the disease. Another factor contributing to the progression of keratoconus is the enzymatic breakdown of collagen fibers within the cornea, causing it to become thinner over time.
Constant eye rubbing can cause micro-damages to the collagen structures within the cornea, accelerating the progression of keratoconus. If you're prone to rubbing your eyes, you might be at a higher risk for this eye condition.
There are several other genetic conditions that may predispose someone to developing keratoconus. These include:
If you're worried that you may have keratoconus or are experiencing symptoms, it's crucial to get a thorough evaluation. Scheduling an eye exam can help determine the best course of treatment for you.