Often appearing in the teens or early twenties, keratoconus is a progressive
disease in which the normally round cornea thins and begins to bulge
into a cone-like shape. This cone shape deflects light as it enters
the eye on its way to the light-sensitive retina, causing distorted
vision. Keratoconus can occur in one or both eyes.
New research has demonstrated a relationship between malfunction of
beneficial enzymes found within the eye's surface and an accompanying
chemical imbalance that leads to toxic damage and thinning of eye
tissue. Because keratoconus can be found in extended families, this
improper functioning of beneficial enzymes appears to have genetic
causes about 5% of the time. Eye damage from keratoconus also can
be linked to factors such as overexposure to sunlight, improper fittings
of contact lenses, excessive eye rubbing, and continual (chronic)
eye irritation.
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